Certain chemical entities, compositions, and methods

ABSTRACT

Chemical entities that modulate smooth muscle myosin and/or non-muscle myosin, pharmaceutical compositions and methods of treatment of diseases and conditions associated with smooth muscle myosin and/or non-muscle myosin are described.

This application is a continuation of U.S. patent application Ser. No. 13/308,287, filed Nov. 30, 2011 now U.S. Pat. No. 8,759,374, which is a continuation of U.S. patent application Ser. No. 12/228,421, filed Aug. 11, 2008, now U.S. Pat. No. 8,088,793, and claims the benefit of U.S. Provisional Patent Application No. 60/965,020, filed Aug. 15, 2007, each of which is hereby incorporated by reference for all purposes.

Provided are certain chemical entities that modulate smooth muscle myosin and/or non-muscle myosin, pharmaceutical compositions and methods of treatment of diseases and conditions associated with smooth muscle myosin and/or non-muscle myosin.

Myosin is present in all muscle and muscle cells. Of the ten distinct classes of myosin in human cells, myosin-II is thought to be the form responsible for contraction of skeletal, cardiac, and smooth muscle. Myosin-II is also the isoform present in non-muscle myosins, also known as cytoplasmic myosins. The non-muscle myosins are ubiquitously present in eukaryotic cells, where the smooth muscle myosins are generally present in smooth muscle cells.

Myosin-II is significantly different in amino acid composition and in overall structure from myosins in the other nine distinct classes. Myosin-II consists of two globular head domains, called Subfragment-1 or S1, linked together by a long alpha-helical coiled-coiled tail. Proteolysis of myosin generates either S1 or heavy meromyosin (HMM, a two-headed form with a truncated tail), depending on the proteolysis conditions. Si contains the ATPase and actin-binding properties of the molecule. S1 has been shown to be sufficient to move actin filaments in vitro, and is therefore likely to be the motor domain of the molecule.

Although myosin-II isoforms from various tissues differ in a number of biological properties, they share the same basic molecular structure as a dimer of two heavy chains (approximately 200 kDa) which are noncovalently associated with two pairs of light chains (approximately 20 and 17 kDa). The two globular amino-terminal heads are tethered together by the carboxy-terminal alpha-helical coiled-coil that forms a tail. The tails are believed to be involved in the assembly of myosin molecules into filaments, whereas the heads are thought to have an actin-activated Mg²⁺-ATPase activity. Each myosin head can be divided by three protease-sensitive regions into peptides of approximately 25, 50, and 20 kDa. The more amino-terminal 25 kDa-50 kDa junction is close to the ATP binding region, whereas the actin-binding domain is near the 50 kDa-20 kDa junction.

S1 consists of a globular actin binding and nucleotide binding region known as the catalytic domain. This domain is attached at its carboxy-terminus to an alpha-helix that has two light chains of about 20 kDa each wrapped around it. This light-chain binding domain of S1 is known as the lever arm. Upon transitioning from the pre-stroke to the post-stroke state, the lever arm is believed to swing through an angle of about 90 degrees about a fulcrum point in the catalytic domain near the nucleotide-binding site. The “power stroke” is driven by the hydrolysis of ATP.

The other end of the myosin molecule is an alpha-helical coiled-coiled tail involved in self assembly of myosin molecules into bipolar thick filaments. These thick filaments interdigitate between thinner actin filaments, and the two filament systems slide past one another during contraction of the muscle. This filament sliding mechanism is thought to involve conformational changes in the myosin heads causing them to walk along the thin actin filaments at the expense of ATP hydrolysis. While non-muscle myosins act in a similar manner, they are understood to slide at a slower velocity than the smooth muscle myosins.

The complete cDNA of the human smooth muscle myosin has been described. The sequence of human smooth muscle myosin is 52% identical to human cardiac myosin in the catalytic S1 region. See, for example, PCT publication No. WO 03/14323.

Provided is at least one chemical entity selected from compounds of Formula I

and pharmaceutically acceptable salts thereof, wherein

W¹ and W² are independently selected from CR¹¹R¹², NR¹³, and O; provided at least one of W¹ and W² is NR¹³;

W³ is selected from CR¹R², NR¹⁴, and O;

Z¹ is selected from heteroaryl and heterocycloalkyl;

Z² is selected from aryl, heteroaryl, and heterocycloalkyl;

R⁸ is selected from hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, and optionally substituted heterocycloalkyl;

R¹, R², R¹¹, and R¹² are independently selected from hydrogen, hydroxy, carboxy, sulfonyl, sulfinyl, sulfanyl, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted alkoxy, optionally substituted aryloxy, optionally substituted heteroaryloxy, optionally substituted heterocycloalkyloxy, optionally substituted aminocarbonyloxy, optionally substituted acyloxy, optionally substituted alkoxycarbonyloxy, optionally substituted alkoxycarbonyl, optionally substituted amino, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aminocarbonyl, and optionally substituted aminosulfonyl; or R¹ and R² may optionally be joined together with any intervening atoms to form a group selected from optionally substituted cycloalkyl and optionally substituted heterocycloalkyl;

R¹³ and R¹⁴ are independently selected from hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, and optionally substituted heterocycloalkyl;

for each occurrence, R³, R⁴, R⁵, and R⁶ are independently selected from hydrogen, hydroxy, carboxy, sulfonyl, sulfinyl, sulfanyl, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted alkoxy, optionally substituted aryloxy, optionally substituted heteroaryloxy, optionally substituted heterocycloalkyloxy, optionally substituted aminocarbonyloxy, optionally substituted acyloxy, optionally substituted alkoxycarbonyloxy, optionally substituted acyl, optionally substituted alkoxycarbonyl, optionally substituted amino, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aminocarbonyl, and optionally substituted aminosulfonyl; or R⁵ and R⁶ taken together form an optionally substituted ring selected from optionally substituted cycloalkyl and optionally substituted heterocycloalkyl.

or R¹ and one occurrence of R⁵ may optionally be joined together with any intervening atoms to form a group selected from optionally substituted cycloalkyl and optionally substituted heterocycloalkyl;

or R¹⁴ and one occurrence of R⁵ may optionally be joined together with any intervening atoms to form an optionally substituted heterocycloalkyl ring;

or if W¹ is NR¹³, then R¹³ and R¹ may optionally be joined together with any intervening atoms to form an optionally substituted heterocycloalkyl ring;

or if W¹ is NR¹³, then R¹³ and one occurrence of R⁵ may optionally be joined together with any intervening atoms to form an optionally substituted heterocycloalkyl ring;

R⁷ and R¹⁰ are independently selected from hydrogen, cyano, halo, hydroxy, azido, nitro, carboxy, sulfinyl, sulfanyl, optionally substituted alkoxy, optionally substituted aryloxy, optionally substituted heteroaryloxy, optionally substituted heterocycloalkyloxy, optionally substituted alkoxycarbonyl, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted aryloxy, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted heterocycloalkyl, optionally substituted amino, optionally substituted acyl, optionally substituted alkoxycarbonyl, optionally substituted aminocarbonyl, optionally substituted aminosulfonyl, optionally substituted carbaminodoyl, and optionally substituted alkynyl;

m is selected from 0, 1, 2, and 3;

n is selected from 0, 1, 2, 3, and 4;

p is selected from 0, 1, 2, and 3; and

q is selected from 1, 2, 3, and 4.

Also provided is a pharmaceutical composition comprising at least one chemical entity described herein, together with at least one pharmaceutically acceptable vehicle selected from carriers, adjuvants, and excipients.

Also provided are methods of treatment of one or more diseases associated with smooth muscle myosin or non-muscle myosin. The methods of treatment comprise administering a therapeutically effective amount of at least one chemical entity provided herein or a pharmaceutical composition comprising at least one chemical entity described herein, together with at least one pharmaceutically acceptable vehicle selected from carriers, adjuvants, and excipients.

Also provided are methods of treating or ameliorating a disease associated with airway wall remodeling in a mammal which method comprises administering to a mammal in need thereof a therapeutically effective amount of at least one chemical entity described herein.

Other aspects and embodiments will be apparent to those skilled in the art from the following detailed description.

As used in the present specification, the following words and phrases are generally intended to have the meanings as set forth below, except to the extent that the context in which they are used indicates otherwise.

The following abbreviations and terms have the indicated meanings throughout:

-   PIPES=1,4-piperazinediethanesulfonic acid -   ATP=adenosine 5′-triphosphate -   DTT=DL-dithiothreitol -   BSA=bovine serum albumin -   NADH=nicotinamide adenine dinucleotide -   PEP=phosphoenolpyruvic acid -   EGTA=ethylene glycol-bis(2-aminoethylether)-N,N,N′,N′-tetraacetic     acid -   Ac=acetyl -   APCI=atmospheric pressure chemical ionization -   atm=atmosphere -   Boc=tert-butoxycarbonyl -   c-=cyclo -   CBZ or Cbz=carbobenzyloxy=benzyloxycarbonyl -   CDI=carbonyldiimidazole -   DCM=dichloromethane=methylene chloride=CH₂Cl₂ -   DIAD=diisopropyl azodicarboxylate -   DIEA=DIPEA=N,N-diisopropylethylamine -   DMAP=4-(dimethylamino)pyridine -   DMF=N,N-dimethylformamide -   DMSO=dimethyl sulfoxide -   (DPPF)PdCl₂=[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) -   Et=ethyl -   EtOAc=ethyl acetate -   EtOH=ethanol -   G or g=gram -   GC=gas chromatograghy -   h or hr=hour -   HATU=O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium     hexafluorophosphate -   HBTU=O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium     hexafluorophosphate -   HOBT=1-hydroxybenzotriazole -   HPLC=high pressure liquid chromatography -   i-=iso -   kg or Kg=kilogram -   L or l=liter -   LC/MS=LCMS=liquid chromatography-mass spectrometry -   LDA=lithium diisopropylamide -   LRMS=low resolution mass spectrometry -   m/z=mass-to-charge ratio -   Me=methyl -   NMP=N-Methyl-2-pyrrolidone -   NMR=nuclear magnetic resonance -   MPLC=medium pressure liquid chromatography -   min=minute -   mL=milliliter -   mol=mole -   mmol=milimole -   MW=microwave -   n-=normal -   Ph=phenyl -   (Ph₃P)₄Pd=tetrakis(triphenylphosphine)palladium(0) -   (Ph₃P)₂PdCl₂=dichlorobis(triphenylphosphine)palladium(II) -   RP-HPLC=reverse phase-high pressure liquid chromatography -   rt or RT=room temperature -   s-=sec-=secondary -   t-=tert-=tertiary -   TBAF=tetrabutylammonium fluoride -   TBS=TBDMS=tert-butyldimethylsilyl -   TES=triethylsilyl or triethylsilane -   TMS=trimethylsilyl or trimethylsilane -   TFA=trifluoroacetic acid -   THF=tetrahydrofuran -   TLC=thin layer chromatography -   UV=ultraviolet -   vol=volume equivalent in mL/g or L/Kg or the limiting reagent unless     otherwise specified

As used herein, when any variable occurs more than one time in a chemical formula, its definition on each occurrence is independent of its definition at every other occurrence.

A dash (“-”) that is not between two letters or symbols is used to indicate a point of attachment for a substituent. For example, —CONH₂ is attached through the carbon atom.

By “optional” or “optionally” is meant that the subsequently described event or circumstance may or may not occur, and that the description includes instances where the event or circumstance occurs and instances in which it does not. For example, “optionally substituted alkyl” encompasses both “alkyl” and “substituted alkyl” as defined below. It will be understood by those skilled in the art, with respect to any group containing one or more substituents, that such groups are not intended to introduce any substitution or substitution patterns that are sterically impractical, synthetically non-feasible and/or inherently unstable.

The term “ATPase,” as used herein, refers to an enzyme that is capable of hydrolyzing ATP. ATPases include proteins comprising molecular motors such as myosins.

“Alkyl” encompasses straight chain and branched chain having the indicated number of carbon atoms, usually from 1 to 20 carbon atoms, for example 1 to 8 carbon atoms, such as 1 to 6 carbon atoms. For example C₁-C₆ alkyl encompasses both straight and branched chain alkyl of from 1 to 6 carbon atoms. When an alkyl residue having a specific number of carbons is named, all branched and straight chain versions having that number of carbons are intended to be encompassed; thus, for example, “butyl” is meant to include n-butyl, sec-butyl, isobutyl and t-butyl; “propyl” includes n-propyl and isopropyl. “Lower alkyl” refers to alkyl groups having one to six carbons. Examples of alkyl groups include methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, pentyl, 2-pentyl, isopentyl, neopentyl, hexyl, 2-hexyl, 3-hexyl, 3-methylpentyl, and the like. Alkylene is a subset of alkyl, referring to the same residues as alkyl, but having two points of attachment. Alkylene groups will usually have from 2 to 20 carbon atoms, for example 2 to 8 carbon atoms, such as from 2 to 6 carbon atoms. For example, C₀ alkylene indicates a covalent bond and C₁ alkylene is a methylene group.

“Alkenyl” refers to an unsaturated branched or straight-chain alkyl group having at least one carbon-carbon double bond derived by the removal of one molecule of hydrogen from adjacent carbon atoms of the parent alkyl. The group may be in either the cis or trans configuration about the double bond(s). Typical alkenyl groups include, but are not limited to, ethenyl; propenyls such as prop-1-en-1-yl, prop-1-en-2-yl, prop-2-en-1-yl(allyl), prop-2-en-2-yl; butenyls such as but-1-en-1-yl, but-1-en-2-yl, 2-methyl-prop-1-en-1-yl, but-2-en-1-yl, but-2-en-1-yl, but-2-en-2-yl, buta-1,3-dien-1-yl, buta-1,3-dien-2-yl; and the like. In certain embodiments, an alkenyl group has from 2 to 20 carbon atoms and in other embodiments, from 2 to 6 carbon atoms. “Lower alkenyl” refers to alkenyl groups having two to six carbons.

“Alkynyl” refers to an unsaturated branched or straight-chain alkyl group having at least one carbon-carbon triple bond derived by the removal of two molecules of hydrogen from adjacent carbon atoms of the parent alkyl. Typical alkynyl groups include, but are not limited to, ethynyl; propynyls such as prop-1-yn-1-yl, prop-2-yn-1-yl; butynyls such as but-1-yn-1-yl, but-1-yn-3-yl, but-3-yn-1-yl; and the like. In certain embodiments, an alkynyl group has from 2 to 20 carbon atoms and in other embodiments, from 3 to 6 carbon atoms. “Lower alkynyl” refers to alkynyl groups having two to six carbons.

“Cycloalkyl” indicates a non-aromatic carbocyclic ring, usually having from 3 to 7 ring carbon atoms. The ring may be saturated or have one or more carbon-carbon double bonds. Examples of cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, and cyclohexenyl, as well as bridged and caged ring groups such as norbornane.

By “alkoxy” is meant an alkyl group of the indicated number of carbon atoms attached through an oxygen bridge such as, for example, methoxy, ethoxy, propoxy, isopropoxy, n-butoxy, sec-butoxy, tert-butoxy, pentyloxy, 2-pentyloxy, isopentyloxy, neopentyloxy, hexyloxy, 2-hexyloxy, 3-hexyloxy, 3-methylpentyloxy, and the like. Alkoxy groups will usually have from 1 to 7 carbon atoms attached through the oxygen bridge. “Lower alkoxy” refers to alkoxy groups having one to six carbons.

“Mono- and di-alkylcarboxamide” encompasses a group of the formula —(C═O)NR_(a)R_(b) where R_(a) and R_(b) are independently selected from hydrogen and alkyl groups of the indicated number of carbon atoms, provided that R_(a) and R_(b) are not both hydrogen.

“Acyl” refers to the groups H—C(O)—; (alkyl)-C(O)—; (cycloalkyl)-C(O)—; (aryl)-C(O)—; (heteroaryl)-C(O)—; and (heterocycloalkyl)-C(O)—, wherein the group is attached to the parent structure through the carbonyl functionality and wherein alkyl, cycloalkyl, aryl, heteroaryl, and heterocycloalkyl are as described herein. Acyl groups have the indicated number of carbon atoms, with the carbon of the keto group being included in the numbered carbon atoms. For example a C₂ acyl group is an acetyl group having the formula CH₃(C═O)—.

“Formyl” refers to the group —C(O)H.

“Carboxy” and/or “carboxyl” refer to the group —C(O)OH.

By “alkoxycarbonyl” is meant a group of the formula (alkoxy)(C═O)— attached through the carbonyl carbon wherein the alkoxy group has the indicated number of carbon atoms. Thus a C₁-C₆ alkoxycarbonyl group is an alkoxy group having from 1 to 6 carbon atoms attached through its oxygen to a carbonyl linker.

By “azido” is meant the group —N₃.

By “amino” is meant the group —NH₂.

“Mono- and di-(alkyl)amino” encompasses secondary and tertiary alkylamino groups, wherein the alkyl groups are as defined above and have the indicated number of carbon atoms. The point of attachment of the alkylamino group is on the nitrogen. Examples of mono- and di-alkylamino groups include ethylamino, dimethylamino, and methyl-propyl-amino.

The term “aminocarbonyl” refers to the group —CONR^(b)R^(c), where

R^(b) is selected from H, optionally substituted C₁-C₆ alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, and optionally substituted heteroaryl, optionally substituted alkoxy; and

R^(c) is independently selected from hydrogen and optionally substituted C₁-C₄ alkyl; or

R^(b) and R^(c) taken together with the nitrogen to which they are bound, form an optionally substituted 5- to 7-membered nitrogen-containing heterocycloalkyl which optionally includes 1 or 2 additional heteroatoms selected from O, N, and S in the heterocycloalkyl ring;

where each substituted group is independently substituted with one or more substituents independently selected from C₁-C₄ alkyl, aryl, heteroaryl, aryl-C₁-C₄ alkyl-, heteroaryl-C₁-C₄ alkyl-, C₁-C₄ haloalkyl, —OC₁-C₄ alkyl, —OC₁-C₄ alkylphenyl, —C₁-C₄ alkyl-OH, —OC₁-C₄ haloalkyl, halo, —OH, —NH₂, —C₁-C₄ alkyl-NH₂, —N(C₁-C₄ alkyl)(C₁-C₄ alkyl), —NH(C₁-C₄ alkyl), —N(C₁-C₄ alkyl)(C₁-C₄ alkylphenyl), —NH(C₁-C₄ alkylphenyl), cyano, nitro, oxo (as a substitutent for cycloalkyl, heterocycloalkyl, or heteroaryl), —CO₂H, —C(O)OC₁-C₄ alkyl, —CON(C₁-C₄ alkyl)(C₁-C₄ alkyl), —CONH(C₁-C₄ alkyl), —CONH₂, —NHC(O)(C₁-C₄ alkyl), —NHC(O)(phenyl), —N(C₁-C₄ alkyl)C(O)(C₁-C₄ alkyl), —N(C₁-C₄ alkyl)C(O)(phenyl), —C(O)C₁-C₄ alkyl, —C(O)C₁-C₄ alkylphenyl, —C(O)C₁-C₄ haloalkyl, —OC(O)C₁-C₄ alkyl, —SO₂(C₁-C₄ alkyl), —SO₂(phenyl), —SO₂(C₁-C₄ haloalkyl), —SO₂NH₂, —SO₂NH(C₁-C₄ alkyl), —SO₂NH(phenyl), —NHSO₂(C₁-C₄ alkyl), —NHSO₂(phenyl), and —NHSO₂(C₁-C₄ haloalkyl).

“Aryl” encompasses:

6-membered carbocyclic aromatic rings, for example, benzene;

bicyclic ring systems wherein at least one ring is carbocyclic and aromatic, for example, naphthalene, indane, and tetralin; and

tricyclic ring systems wherein at least one ring is carbocyclic and aromatic, for example, fluorene.

For example, aryl includes 6-membered carbocyclic aromatic rings fused to a 5- to 7-membered heterocycloalkyl ring containing 1 or more heteroatoms selected from N, O, and S. For such fused, bicyclic ring systems wherein only one of the rings is a carbocyclic aromatic ring, the point of attachment may be at the carbocyclic aromatic ring or the heterocycloalkyl ring. Bivalent radicals formed from substituted benzene derivatives and having the free valences at ring atoms are named as substituted phenylene radicals. Bivalent radicals derived from univalent polycyclic hydrocarbon radicals whose names end in “-yl” by removal of one hydrogen atom from the carbon atom with the free valence are named by adding “-idene” to the name of the corresponding univalent radical, e.g. a naphthyl group with two points of attachment is termed naphthylidene. Aryl, however, does not encompass or overlap in any way with heteroaryl, separately defined below. Hence, if one or more carbocyclic aromatic rings is fused with a heterocycloalkyl aromatic ring, the resulting ring system is heteroaryl, not aryl, as defined herein.

The term “aryloxy” refers to the group —O-aryl.

The term “aralkyl” refers to the group -alkyl-aryl.

“Carbamimidoyl” refers to the group —C(═NH)—NH2.

“Substituted carbamimidoyl” refers to the group —C(═NR^(e))—NR^(f)R^(g) where

R^(e) is selected from hydrogen, cyano, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, and optionally substituted heterocycloalkyl; and

R^(f) and R^(g) are independently selected from hydrogen optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, and optionally substituted heterocycloalkyl,

provided that at least one of R^(e), R^(f), and R^(g) is not hydrogen and wherein substituted alkyl, cycloalkyl, aryl, heterocycloalkyl, and heteroaryl refer respectively to alkyl, cycloalkyl, aryl, heterocycloalkyl, and heteroaryl wherein one or more (such as up to 5, for example, up to 3) hydrogen atoms are replaced by a substituent independently selected from

—R^(a), —OR^(b), optionally substituted amino (including —NR^(c)COR^(b), —NR^(c)CO₂R^(a), —NR^(c)CONR^(b)R^(c), —NR^(b)C(NR^(c))NR^(b)R^(c), —NR^(b)C(NCN)NR^(b)R^(C), and —NR^(c)SO₂R^(a)), halo, cyano, nitro, oxo (as a substitutent for cycloalkyl, heterocycloalkyl, and heteroaryl), optionally substituted acyl (such as —COR^(b)), optionally substituted alkoxycarbonyl (such as —CO₂R^(b)), aminocarbonyl (such as —CONR^(b)R^(c)), —OCOR^(b), —OCO₂R^(a), —OCONR^(b)R^(c), sulfanyl (such as SR^(b)), sulfinyl (such as —SOR^(a)), and sulfonyl (such as —SO₂R^(a) and —SO₂NR^(b)R^(c)),

where R^(a) is selected from optionally substituted C1-C6 alkyl, optionally substituted aryl, and optionally substituted heteroaryl;

R^(b) is selected from H, optionally substituted C1-C6 alkyl, optionally substituted aryl, and optionally substituted heteroaryl; and

R^(c) is independently selected from hydrogen and optionally substituted C1-C4 alkyl; or

R^(b) and R^(c), and the nitrogen to which they are attached, form an optionally substituted heterocycloalkyl group; and

where each optionally substituted group is unsubstituted or independently substituted with one or more, such as one, two, or three, substituents independently selected from C₁-C₄ alkyl, aryl, heteroaryl, aryl-C₁-C₄ alkyl-, heteroaryl-C₁-C₄ alkyl-, C₁-C₄ haloalkyl, —OC₁-C₄ alkyl, —OC₁-C₄ alkylphenyl, —C₁-C₄ alkyl-OH, —OC₁-C₄ haloalkyl, halo, —OH, —NH₂, —C₁-C₄ alkyl-NH₂, —N(C₁-C₄ alkyl)(C₁-C₄ alkyl), —NH(C₁-C₄ alkyl), —N(C₁-C₄ alkyl)(C₁-C₄ alkylphenyl), —NH(C₁-C₄ alkylphenyl), cyano, nitro, oxo (as a substitutent for cycloalkyl, heterocycloalkyl, or heteroaryl), —CO₂H, —C(O)OC₁-C₄ alkyl, —CON(C₁-C₄ alkyl)(C₁-C₄ alkyl), —CONH(C₁-C₄ alkyl), —CONH₂, —NHC(O)(C₃-C₄ alkyl), —NHC(O)(phenyl), —N(C₁-C₄ alkyl)C(O)(C₁-C₄ alkyl), —N(C₁-C₄ alkyl)C(O)(phenyl), —C(O)C₁-C₄ alkyl, —C(O)C₁-C₄ phenyl, —C(O)C₁-C₄ haloalkyl, —OC(O)C₁-C₄ alkyl, —SO₂(C₁-C₄ alkyl), —SO₂(phenyl), —SO₂(C₁-C₄ haloalkyl), —SO₂NH₂, —SO₂NH(C₁-C₄ alkyl), —SO₂ NH(phenyl), —NHSO₂(C₁-C₄ alkyl), —NHSO₂(phenyl), and —NHSO₂(C₁-C₄ haloalkyl).

The term “halo” includes fluoro, chloro, bromo, and iodo, and the term “halogen” includes fluorine, chlorine, bromine, and iodine.

“Haloalkyl” indicates alkyl as defined above having the specified number of carbon atoms, substituted with 1 or more halogen atoms, up to the maximum allowable number of halogen atoms. Examples of haloalkyl include, but are not limited to, trifluoromethyl, difluoromethyl, 2-fluoroethyl, and penta-fluoroethyl.

“Heteroaryl” encompasses:

5- to 7-membered aromatic, monocyclic rings containing one or more, for example, from 1 to 4, or in certain embodiments, from 1 to 3, heteroatoms selected from N, O, and S, with the remaining ring atoms being carbon;

bicyclic heterocycloalkyl rings containing one or more, for example, from 1 to 4, or in certain embodiments, from 1 to 3, heteroatoms selected from N, O, and S, with the remaining ring atoms being carbon and wherein at least one heteroatom is present in an aromatic ring; and

tricyclic heterocycloalkyl rings containing one or more, for example, from 1 to 5, or in certain embodiments, from 1 to 4, heteroatoms selected from N, O, and S, with the remaining ring atoms being carbon and wherein at least one heteroatom is present in an aromatic ring.

For example, heteroaryl includes a 5- to 7-membered heterocycloalkyl, aromatic ring fused to a 5- to 7-membered cycloalkyl or heterocycloalkyl ring. For such fused, bicyclic heteroaryl ring systems wherein only one of the rings contains one or more heteroatoms, the point of attachment may be at either ring. When the total number of S and O atoms in the heteroaryl group exceeds 1, those heteroatoms are not adjacent to one another. In certain embodiments, the total number of S and O atoms in the heteroaryl group is not more than 2. In certain embodiments, the total number of S and O atoms in the aromatic heterocycle is not more than 1. Examples of heteroaryl groups include, but are not limited to, (as numbered from the linkage position assigned priority 1), 2-pyridyl, 3-pyridyl, 4-pyridyl, 2,3-pyrazinyl, 3,4-pyrazinyl, 2,4-pyrimidinyl, 3,5-pyrimidinyl, 2,3-pyrazolinyl, 2,4-imidazolinyl, isoxazolinyl, oxazolinyl, thiazolinyl, thiadiazolinyl, tetrazolyl, thienyl, benzothiophenyl, furanyl, benzofuranyl, benzoimidazolinyl, indolinyl, pyridazinyl, triazolyl, quinolinyl, pyrazolyl, and 5,6,7,8-tetrahydroisoquinolinyl. Other examples of heteroaryl groups include, but are not limited to, isoquinolinyl, isoxazol-3-yl, and isoxazol-5-yl. Bivalent radicals derived from univalent heteroaryl radicals whose names end in “-yl” by removal of one hydrogen atom from the atom with the free valence are named by adding “-idene” to the name of the corresponding univalent radical, e.g. a pyridyl group with two points of attachment is a pyridylidene. Heteroaryl does not encompass or overlap with aryl, cycloalkyl, or heterocycloalkyl, as defined herein

Substituted heteroaryl also includes ring systems substituted with one or more oxide (—O⁻) substituents, such as pyridinyl N-oxides.

By “heterocycloalkyl” is meant a single, non-aromatic ring, usually with 3 to 7 ring atoms, containing at least 2 carbon atoms in addition to 1-3 heteroatoms independently selected from oxygen, sulfur, and nitrogen, as well as combinations comprising at least one of the foregoing heteroatoms. The ring may be saturated or have one or more carbon-carbon double bonds. Suitable heterocycloalkyl groups include, for example (as numbered from the linkage position assigned priority 1), 2-pyrrolidinyl, 2,4-imidazolidinyl, 2,3-pyrazolidinyl, 2-piperidyl, 3-piperidyl, 4-piperidyl, and 2,5-piperizinyl. Morpholinyl groups are also contemplated, including 2-morpholinyl and 3-morpholinyl (numbered wherein the oxygen is assigned priority 1). Substituted heterocycloalkyl also includes ring systems substituted with one or more oxo (═O) or oxide (—O⁻) substituents, such as piperidinyl N-oxide, morpholinyl-N-oxide, 1-oxo-1-thiomorpholinyl and 1,1-dioxo-1-thiomorpholinyl.

“Heterocycloalkyl” also includes bicyclic ring systems wherein one non-aromatic ring, usually with 3 to 7 ring atoms, contains at least 2 carbon atoms in addition to 1-3 heteroatoms independently selected from oxygen, sulfur, and nitrogen, as well as combinations comprising at least one of the foregoing heteroatoms; and the other ring, usually with 3 to 7 ring atoms, optionally contains 1-3 heteratoms independently selected from oxygen, sulfur, and nitrogen and is not aromatic.

As used herein, “modulation” refers to a change in activity as a direct or indirect response to the presence of a chemical entity as described herein, relative to the activity of in the absence of the chemical entity. The change may be an increase in activity or a decrease in activity, and may be due to the direct interaction of the compound with the a target or due to the interaction of the compound with one or more other factors that in turn affect the target's activity. For example, the presence of the chemical entity may, for example, increase or decrease the target activity by directly binding to the target, by causing (directly or indirectly) another factor to increase or decrease the target activity, or by (directly or indirectly) increasing or decreasing the amount of target present in the cell or organism.

The term “sulfanyl” includes the groups: —S-(optionally substituted (C₁-C₆)alkyl), —S-(optionally substituted aryl), —S-(optionally substituted heteroaryl), and —S-(optionally substituted heterocycloalkyl). Hence, sulfanyl includes the group C₁-C₆ alkylsulfanyl.

The term “sulfinyl” includes the groups: —S(O)-(optionally substituted (C₁-C₆)alkyl), —S(O)-optionally substituted aryl), —S(O)-optionally substituted heteroaryl), —S(O)-(optionally substituted heterocycloalkyl); and —S(O)-(optionally substituted amino).

The term “sulfonyl” includes the groups: —S(O₂)-(optionally substituted (C₁-C₆)alkyl), —S(O₂)-optionally substituted aryl), —S(O₂)-optionally substituted heteroaryl), —S(O₂)-(optionally substituted heterocycloalkyl), and —S(O₂)-(optionally substituted amino).

The term “substituted”, as used herein, means that any one or more hydrogens on the designated atom or group is replaced with a selection from the indicated group, provided that the designated atom's normal valence is not exceeded. When a substituent is oxo (i.e. ═O) then 2 hydrogens on the atom are replaced. Combinations of substituents and/or variables are permissible only if such combinations result in stable compounds or useful synthetic intermediates. A stable compound or stable structure is meant to imply a compound that is sufficiently robust to survive isolation from a reaction mixture, and subsequent formulation as an agent having at least practical utility. Unless otherwise specified, substituents are named into the core structure. For example, it is to be understood that when (cycloalkyl)alkyl is listed as a possible substituent, the point of attachment of this substituent to the core structure is in the alkyl portion.

The terms “substituted” alkyl, cycloalkyl, aryl, heterocycloalkyl, and heteroaryl, unless otherwise expressly defined, refer respectively to alkyl, cycloalkyl, aryl, heterocycloalkyl, and heteroaryl wherein one or more (such as up to 5, for example, up to 3) hydrogen atoms are replaced by a substituent independently selected from

—R^(a), —OR^(b), optionally substituted amino (including —NR^(c)OR^(b), —NR^(c)CO₂R^(a), —NR^(c)CONR^(b)R^(c), NR^(b)C(NR^(c))NR^(b)R^(c), NR^(b)C(NCN)NR^(b)R^(c), —NR^(b)C(NH₂)NC(O)NH₂, —NR^(b)C(NH₂)N(CN), and —NR^(c)SO₂R^(a)), halo, cyano, azido, nitro, oxo (as a substitutent for cycloalkyl or heterocycloalkyl), optionally substituted acyl (such as —COR^(b)), optionally substituted alkoxycarbonyl (such as —CO₂R^(b)), aminocarbonyl (such as —CONR^(b)R^(c)), —OCOR^(b), —OCO₂R^(a), —OCONR^(b)R^(c), —OP(O)(OR^(b))OR^(c), sulfanyl (such as SR^(b)), sulfinyl (such as —SOR^(a)), and sulfonyl (such as —SO₂R^(a) and —SO₂NR^(b)R^(c)),

where R^(a) is selected from optionally substituted C₁-C₆ alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, and optionally substituted heteroaryl;

R^(b) is selected from hydrogen, optionally substituted C₁-C₆ alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, and optionally substituted heteroaryl; and

R^(c) is independently selected from hydrogen and optionally substituted C₁-C₄ alkyl; or

R^(b) and R^(c), and the nitrogen to which they are attached, form an optionally substituted heterocycloalkyl group; and

where each optionally substituted group is unsubstituted or independently substituted with one or more, such as one, two, or three, substituents independently selected from C₁-C₄ alkyl, aryl, heteroaryl, aryl-C₁-C₄ alkyl-, heteroaryl-C₁-C₄ alkyl-, C₁-C₄ haloalkyl, —OC₁-C₄ alkyl, —OC₁-C₄ alkylphenyl, —C₁-C₄ alkyl-OH, —OC₁-C₄ haloalkyl, halo, —OH, —NH₂, —C₁-C₄ alkyl-NH₂, —N(C₁-C₄ alkyl)(C₁-C₄ alkyl), —NH(C₁-C₄ alkyl), —N(C₁-C₄ alkyl)(C₁-C₄ alkylphenyl), —NH(C₁-C₄ alkylphenyl), cyano, nitro, oxo (as a substitutent for cycloalkyl or heterocycloalkyl), —CO₂H, —C(O)OC₁-C₄ alkyl, —CON(C₁-C₄ alkyl)(C₁-C₄ alkyl), —CONH(C₁-C₄ alkyl), —CONH₂, —NHC(O)(C₁-C₄ alkyl), —NHC(O)(phenyl), —N(C₁-C₄ alkyl)C(O)(C₁-C₄ alkyl), —N(C₁-C₄ alkyl)C(O)(phenyl), —C(O)C₁-C₄ alkyl, —C(O)C₁-C₄ alkylphenyl, —C(O)C₁-C₄ haloalkyl, —OC(O)C₁-C₄ alkyl, —SO₂(C₁-C₄ alkyl), —SO₂(phenyl), —SO₂(C₁-C₄ haloalkyl), —SO₂NH₂, —SO₂NH(C₁-C₄ alkyl), —SO₂NH(phenyl), —NHSO₂(C₁-C₄ alkyl), —NHSO₂(phenyl), and —NHSO₂(C₁-C₄ haloalkyl).

The term “substituted acyl” refers to the groups (substituted alkyl)-C(O)—; (substituted cycloalkyl)-C(O)—; (substituted aryl)-C(O)—; (substituted heteroaryl)-C(O)—; and (substituted heterocycloalkyl)-C(O)—, wherein the group is attached to the parent structure through the carbonyl functionality and wherein substituted alkyl, cycloalkyl, aryl, heteroaryl, and heterocycloalkyl, refer respectively to alkyl, cycloalkyl, aryl, heteroaryl, and heterocycloalkyl wherein one or more (such as up to 5, for example, up to 3) hydrogen atoms are replaced by a substituent independently selected from

—R^(a), —OR^(b), optionally substituted amino (including —NR^(c)COR^(b), —NR^(c)CO₂R^(a), —NR^(c)CONR^(b)R^(c), —NR^(b)C(NR^(c))NR^(b)R^(c), —NR^(b)C(NCN)NR^(b)R^(c), and —NR^(c)SO₂R^(a)), halo, cyano, nitro, oxo (as a substitutent for cycloalkyl or heterocycloalkyl), optionally substituted acyl (such as —COR^(b)), optionally substituted alkoxycarbonyl (such as —CO₂R^(b)), aminocarbonyl (such as —CONR^(b)R^(c)), —OCOR^(b), —OCO₂R^(a), —OCONR^(b)R^(c), —OP(O)(OR^(b))OR^(c), sulfanyl (such as SR^(b)), sulfinyl (such as —SOR^(a)), and sulfonyl (such as —SO₂R^(a) and —SO₂NR^(b)R^(c)), where R^(a) is selected from optionally substituted C₁-C₆ alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, and optionally substituted heteroaryl;

R^(b) is selected from H, optionally substituted C₁-C₆ alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, and optionally substituted heteroaryl; and

R^(c) is independently selected from hydrogen and optionally substituted C₁-C₄ alkyl; or

R^(b) and R^(c), and the nitrogen to which they are attached, form an optionally substituted heterocycloalkyl group; and

where each optionally substituted group is unsubstituted or independently substituted with one or more, such as one, two, or three, substituents independently selected from C₁-C₄ alkyl, aryl, heteroaryl, aryl-C₁-C₄ alkyl-, heteroaryl-C₁-C₄ alkyl-, C₁-C₄ haloalkyl, —OC₁-C₄ alkyl, —OC₁-C₄ alkylphenyl, —C₁-C₄ alkyl-OH, —OC₁-C₄ haloalkyl, halo, —OH, —NH₂, —C₁-C₄ alkyl-NH₂, —N(C₁-C₄ alkyl)(C₁-C₄ alkyl), —NH(C₁-C₄ alkyl), —N(C₁-C₄ alkyl)(C₁-C₄ alkylphenyl), —NH(C₁-C₄ alkylphenyl), cyano, nitro, oxo (as a substituent for cycloalkyl or heterocycloalkyl), —CO₂H, —C(O)OC₁-C₄ alkyl, —CON(C₁-C₄ alkyl)(C₁-C₄ alkyl), —CONH(C₁-C₄ alkyl), —CONH₂, —NHC(O)(C₁-C₄ alkyl), —NHC(O)(phenyl), —N(C₁-C₄ alkyl)C(O)(C₁-C₄ alkyl), —N(C₁-C₄ alkyl)C(O)(phenyl), —C(O)C₁-C₄ alkyl, —C(O)C₁-C₄ alkylphenyl, —C(O)C₁-C₄ haloalkyl, —OC(O)C₁-C₄ alkyl, —SO₂(C₁-C₄ alkyl), —SO₂(phenyl), —SO₂(C₁-C₄ haloalkyl), —SO₂NH₂, —SO₂NH(C₁-C₄ alkyl), —SO₂NH(phenyl), —NHSO₂(C₁-C₄ alkyl), —NHSO₂(phenyl), and —NHSO₂(C₁-C₄ haloalkyl).

The term “substituted alkoxy” refers to alkoxy wherein the alkyl constituent is substituted (i.e. —O-(substituted alkyl)) wherein “substituted alkyl” refers to alkyl wherein one or more (such as up to 5, for example, up to 3) hydrogen atoms are replaced by a substituent independently selected from

—R^(a), —OR^(b), optionally substituted amino (including —NR^(c)COR^(b), —NR^(c)CO₂R^(a), —NR^(c)CONR^(b)R^(c), —NR^(b)C(NR^(c))NR^(b)R^(c), —NR^(b)C(NCN)NR^(b)R^(c), and —NR^(c)SO₂R^(a)), halo, cyano, nitro, oxo (as a substitutent for cycloalkyl or heterocycloalkyl), optionally substituted acyl (such as —COR^(b)), optionally substituted alkoxycarbonyl (such as —CO₂R^(b)), aminocarbonyl (such as —CONR^(b)R^(c)), —OCOR^(b), —OCO₂R^(a), —OCONR^(b)R^(c), —OP(O)(OR^(b))OR^(c), sulfanyl (such as SR^(b)), sulfinyl (such as —SOR^(a)), and sulfonyl (such as —SO₂R^(a) and —SO₂NR^(b)R^(c)),

where R^(a) is selected from optionally substituted C₁-C₆ alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, and optionally substituted heteroaryl;

R^(b) is selected from H, optionally substituted C₁-C₆ alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, and optionally substituted heteroaryl; and

R^(c) is independently selected from hydrogen and optionally substituted C₁-C₄ alkyl; or

R^(b) and R^(c), and the nitrogen to which they are attached, form an optionally substituted heterocycloalkyl group; and

where each optionally substituted group is unsubstituted or independently substituted with one or more, such as one, two, or three, substituents independently selected from C₁-C₄ alkyl, aryl, heteroaryl, aryl-C₁-C₄ alkyl-, heteroaryl-C₁-C₄ alkyl-, C₁-C₄ haloalkyl, —OC₁-C₄ alkyl, —OC₁-C₄ alkylphenyl, —C₁-C₄ alkyl-OH, —OC₁-C₄ haloalkyl, halo, —OH, —NH₂, —C₁-C₄ alkyl-NH₂, —N(C₁-C₄ alkyl)(C₁-C₄ alkyl), —NH(C₁-C₄ alkyl), —N(C₁-C₄ alkyl)(C₁-C₄ alkylphenyl), —NH(C₁-C₄ alkylphenyl), cyano, nitro, oxo (as a substitutent for cycloalkyl or heterocycloalkyl), —CO₂H, —C(O)OC₁-C₄ alkyl, —CON(C₁-C₄ alkyl)(C₁-C₄ alkyl), —CONH(C₁-C₄ alkyl), —CONH₂, —NHC(O)(C₁-C₄ alkyl), —NHC(O)(phenyl), —N(C₁-C₄ alkyl)C(O)(C₁-C₄ alkyl), —N(C₁-C₄ alkyl)C(O)(phenyl), —C(O)C₁-C₄ alkyl, —C(O)C₁-C₄ alkylphenyl, —C(O)C₁-C₄ haloalkyl, —OC(O)C₁-C₄ alkyl, —SO₂(C₁-C₄ alkyl), —SO₂(phenyl), —SO₂(C₁-C₄ haloalkyl), —SO₂NH₂, —SO₂NH(C₁-C₄ alkyl), —SO₂NH(phenyl), —NHSO₂(C₁-C₄ alkyl), —NHSO₂(phenyl), and —NHSO₂(C₁-C₄ haloalkyl).

In some embodiments, a substituted alkoxy group is “polyalkoxy” or —O-(optionally substituted alkylene)-(optionally substituted alkoxy), and includes groups such as —OCH2CH2OCH3, and residues of glycol ethers such as polyethyleneglycol, and —O(CH2CH2O)xCH3, where x is an integer of 2-20, such as 2-10, and for example, 2-5. Another substituted alkoxy group is hydroxyalkoxy or —OCH2(CH2)yOH, where y is an integer of 1-10, such as 1-4.

The term “substituted alkoxycarbonyl” refers to the group (substituted alkyl)-O—C(O)— wherein the group is attached to the parent structure through the carbonyl functionality and wherein substituted refers to alkyl wherein one or more (such as up to 5, for example, up to 3) hydrogen atoms are replaced by a substituent independently selected from

—R^(a), —OR^(b), optionally substituted amino (including —NR^(c)COR^(b), —NR^(c)CO₂R^(a), —NR^(c)CONR^(b)R^(c), —NR^(b)C(NR^(c))NR^(b)R^(c), —NR^(b)c(NCN)NR^(b)R^(c), and —NR^(c)SO₂R^(a)), halo, cyano, nitro, oxo (as a substitutent for cycloalkyl or heterocycloalkyl), optionally substituted acyl (such as —COR^(b)), optionally substituted alkoxycarbonyl (such as —CO₂R^(b)), aminocarbonyl (such as —CONR^(b)R^(c)), —OCOR^(b), —OCO₂R^(c), —OCONR^(b)R^(c), —OP(O)(OR^(b))OR^(c), sulfanyl (such as SR^(b)), sulfinyl (such as —SOR^(a)), and sulfonyl (such as —SO₂R^(a) and —SO₂NR^(b)R^(c)),

where R^(a) is selected from optionally substituted C₁-C₆ alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, and optionally substituted heteroaryl;

R^(b) is selected from H, optionally substituted C₁-C₆ alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, and optionally substituted heteroaryl; and

R^(c) is independently selected from hydrogen and optionally substituted C₁-C₄ alkyl; or

R^(b) and R^(c), and the nitrogen to which they are attached, form an optionally substituted heterocycloalkyl group; and

where each optionally substituted group is unsubstituted or independently substituted with one or more, such as one, two, or three, substituents independently selected from C₁-C₄ alkyl, aryl, heteroaryl, aryl-C₁-C₄ alkyl-, heteroaryl-C₁-C₄ alkyl-, C₁-C₄ haloalkyl, —OC₁-C₄ alkyl, —OC₁-C₄ alkylphenyl, —C₁-C₄ alkyl-OH, —OC₁-C₄ haloalkyl, halo, —OH, —NH₂, —C₁-C₄ alkyl-NH₂, —N(C₁-C₄ alkyl)(C₁-C₄ alkyl), —NH(C₁-C₄ alkyl), —N(C₁-C₄ alkyl)(C₁-C₄ alkylphenyl), —NH(C₁-C₄ alkylphenyl), cyano, nitro, oxo (as a substitutent for cycloalkyl or heterocycloalkyl), —CO₂H, —C(O)OC₁-C₄ alkyl, —CON(C₁-C₄ alkyl)(C₁-C₄ alkyl), —CONH(C₁-C₄ alkyl), —CONH₂, —NHC(O)(C₁-C₄ alkyl), —NHC(O)(phenyl), —N(C₄-C₄ alkyl)C(O)(C₁-C₄ alkyl), —N(C₁-C₄ alkyl)C(O)(phenyl), —C(O)C₁-C₄ alkyl, —C(O)C₁-C₄ alkylphenyl, —C(O)C₁-C₄haloalkyl, —OC(O)C₁-C₄ alkyl, —SO₂(C₁-C₄ alkyl), —SO₂(phenyl), —SO₂(C₁-C₄ haloalkyl), —SO₂NH₂, —SO₂NH(C₁-C₄ alkyl), —SO₂NH(phenyl), —NHSO₂(C₁-C₄ alkyl), —NHSO₂(phenyl), and —NHSO₂(C₁-C₄ haloalkyl).

The term “substituted amino” refers to the group —NHR^(d) or —NR^(d)R^(e) wherein R^(d) is selected from hydroxy, formyl, optionally substituted alkoxy, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted acyl, optionally substituted carbamimidoyl, aminocarbonyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted heterocycloalkyl, optionally substituted alkoxycarbonyl, sulfinyl and sulfonyl, and wherein R^(e) is selected from optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, and optionally substituted heterocycloalkyl, and wherein substituted alkyl, cycloalkyl, aryl, heterocycloalkyl, and heteroaryl refer respectively to alkyl, cycloalkyl, aryl, heterocycloalkyl, and heteroaryl wherein one or more (such as up to 5, for example, up to 3) hydrogen atoms are replaced by a substituent independently selected from

—R^(a), —OR^(b), optionally substituted amino (including —NR^(c)COR^(b), —NR^(c)CO₂R^(a), —NR^(c)CONR^(b)R^(c), —NR^(b)C(NR^(c))NR^(b)R^(c), NR^(b)C(NCN)NR^(b)R^(c), and —NR^(c)SO₂R^(a)), halo, cyano, nitro, oxo (as a substitutent for cycloalkyl or heterocycloalkyl), optionally substituted acyl (such as —COR^(b)), optionally substituted alkoxycarbonyl (such as —CO₂R^(b)), aminocarbonyl (such as —CONR^(b)R^(c)), —OCOR^(b), —OCO₂R^(d), —OCONR^(b)R^(c), —OP(O)(OR^(b))OR^(c), sulfanyl (such as SR^(b)), sulfinyl (such as —SOR^(a)), and sulfonyl (such as —SO₂R^(a) and —SO₂NR^(b)R^(c)),

where R^(a) is selected from optionally substituted C₁-C₆ alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, and optionally substituted heteroaryl;

R^(b) is selected from H, optionally substituted C₁-C₆ alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, and optionally substituted heteroaryl; and

R^(c) is independently selected from hydrogen and optionally substituted C₁-C₄ alkyl; or

R^(b) and R^(c), and the nitrogen to which they are attached, form an optionally substituted heterocycloalkyl group; and

where each optionally substituted group is unsubstituted or independently substituted with one or more, such as one, two, or three, substituents independently selected from C₁-C₄ alkyl, aryl, heteroaryl, aryl-C₁-C₄ alkyl-, heteroaryl-C₁-C₄ alkyl-, C₁-C₄ haloalkyl, —OC₁-C₄ alkyl, —OC₁-C₄ alkylphenyl, —C₁-C₄ alkyl-OH, —OC₁-C₄ haloalkyl, halo, —OH, —NH₂, —C₁-C₄ alkyl-NH₂, —N(C₁-C₄ alkyl)(C₁-C₄ alkyl), —NH(C₁-C₄ alkyl), —N(C₁-C₄ alkyl)(C₄-C₄ alkylphenyl), —NH(C₁-C₄ alkylphenyl), cyano, nitro, oxo (as a substitutent for cycloalkyl or heterocycloalkyl), —CO₂H, —C(O)OC₁-C₄ alkyl, —CON(C₁-C₄ alkyl)(C₁-C₄ alkyl), —CONH(C₁-C₄ alkyl), —CONH₂, —NHC(O)(C₁-C₄ alkyl), —NHC(O)(phenyl), —N(C₁-C₄ alkyl)C(O)(C₁-C₄ alkyl), —N(C₁-C₄ alkyl)C(O)(phenyl), —C(O)C₁-C₄ alkyl, —C(O)C₁-C₄ alkylphenyl, —C(O)C₁-C₄ haloalkyl, —OC(O)C₁-C₄ alkyl, —SO₂(C₁-C₄ alkyl), —SO₂(phenyl), —SO₂(C₁-C₄ haloalkyl), —SO₂NH₂, —SO₂NH(C₁-C₄ alkyl), —SO₂NH(phenyl), —NHSO₂(C₁-C₄ alkyl), —NHSO₂(phenyl), and —NHSO₂(C₁-C₄ haloalkyl); and

wherein optionally substituted acyl, optionally substituted alkoxycarbonyl, sulfinyl and sulfonyl are as defined herein.

The term “substituted amino” also refers to N-oxides of the groups —NHR^(d), and NR^(d)R^(d) each as described above. N-oxides can be prepared by treatment of the corresponding amino group with, for example, hydrogen peroxide or m-chloroperoxybenzoic acid. The person skilled in the art is familiar with reaction conditions for carrying out the N-oxidation.

The term “phosphato” refers to —OP(O)(OR^(b))OR^(c) where R^(b) is selected from hydrogen, optionally substituted C₁-C₆ alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, and optionally substituted heteroaryl; and R^(c) is independently selected from hydrogen and optionally substituted C₁-C₄ alkyl. In some embodiments, R^(b) and R^(c) are hydrogen.

Compounds of Formula I include, but are not limited to, optical isomers of compounds of Formula I, racemates, and other mixtures thereof. In those situations, the single enantiomers or diastereomers, i.e. optically active forms, can be obtained by asymmetric synthesis or by resolution of the racemates. Resolution of the racemates can be accomplished, for example, by conventional methods such as crystallization in the presence of a resolving agent, or chromatography, using, for example a chiral high-pressure liquid chromatography (HPLC) column. In addition, compounds of Formula I include Z- and E-forms (or cis- and trans-forms) of compounds with carbon-carbon double bonds. Where compounds of Formula I exists in various tautomeric forms, chemical entities described herein include all tautomeric forms of the compound.

Chemical entities described herein include, but are not limited to compounds of Formula I and all pharmaceutically acceptable forms thereof. Pharmaceutically acceptable forms of the chemical entities recited herein include pharmaceutically acceptable salts, solvates, crystal forms (including polymorphs and clathrates), chelates, non-covalent complexes, prodrugs, and mixtures thereof. In certain embodiments, the chemical entities described herein are in the form of pharmaceutically acceptable salts. Hence, the terms “chemical entity” and “chemical entities” also encompass pharmaceutically acceptable salts, solvates, chelates, non-covalent complexes, prodrugs, and mixtures.

“Pharmaceutically acceptable salts” include, but are not limited to salts with inorganic acids, such as hydrochloride, phosphate, diphosphate, hydrobromide, sulfate, sulfinate, nitrate, and like salts; as well as salts with an organic acid, such as malate, maleate, fumarate, tartrate, succinate, citrate, lactate, methanesulfonate, p-toluenesulfonate, 2-hydroxyethylsulfonate, benzoate, salicylate, stearate, and alkanoate such as acetate, HOOC—(CH₂)_(n)—COOH where n is 0-4, and like salts. Similarly, pharmaceutically acceptable cations include, but are not limited to sodium, potassium, calcium, aluminum, lithium, and ammonium.

In addition, if the compound of Formula I is obtained as an acid addition salt, the free base can be obtained by basifying a solution of the acid salt. Conversely, if the product is a free base, an addition salt, particularly a pharmaceutically acceptable addition salt, may be produced by dissolving the free base in a suitable organic solvent and treating the solution with an acid, in accordance with conventional procedures for preparing acid addition salts from base compounds. Those skilled in the art will recognize various synthetic methodologies that may be used to prepare non-toxic pharmaceutically acceptable addition salts.

As noted above, prodrugs also fall within the scope of chemical entities, for example ester or amide derivatives of the compounds of Formula I. The term “prodrugs” includes any chemical entities that become compounds of Formula I when administered to a patient, e.g. upon metabolic processing of the prodrug. Examples of prodrugs include, but are not limited to, acetate, formate, phosphate, and benzoate and like derivatives of functional groups (such as alcohol or amine groups) in the compounds of Formula I.

The term “solvate” refers to the chemical entity formed by the interaction of a solvent and a compound. Suitable solvates are pharmaceutically acceptable solvates, such as hydrates, including monohydrates and hemi-hydrates.

The term “chelate” refers to the chemical entity formed by the coordination of a compound to a metal ion at two (or more) points.

The term “non-covalent complex” refers to the chemical entity formed by the interaction of a compound and another molecule wherein a covalent bond is not formed between the compound and the molecule. For example, complexation can occur through van der Waals interactions, hydrogen bonding, and electrostatic interactions (also called ionic bonding).

The term “active agent” is used to indicate a chemical entity which has biological activity. In certain embodiments, an “active agent” is a compound having pharmaceutical utility. For example an active agent may be an anti-cancer therapeutic.

By “significant” is meant any detectable change that is statistically significant in a standard parametric test of statistical significance such as Student's T-test, where p<0.05.

The term “therapeutically effective amount” of a chemical entity described herein means an amount effective, when administered to a human or non-human patient, to provide a therapeutic benefit such as amelioration of symptoms, slowing of disease progression, or prevention of disease.

“Treatment” or “treating” means any treatment of a disease in a patient, including:

-   -   a) preventing the disease, that is, causing the clinical         symptoms of the disease not to develop;     -   b) inhibiting the disease;     -   c) slowing or arresting the development of clinical symptoms;         and/or     -   d) relieving the disease, that is, causing the regression of         clinical symptoms.

“Patient” refers to an animal, such as a mammal, that has been or will be the object of treatment, observation or experiment. The methods described herein can be useful in both human therapy and veterinary applications. In some embodiments, the patient is a mammal; in some embodiments the patient is human; and in some embodiments the patient is selected from cats and dogs.

Provided is at least one chemical entity selected from compounds of Formula I

and pharmaceutically acceptable salts thereof, wherein

W¹ and W² are independently selected from CR¹¹R¹², NR¹³, and O; provided at least one of W¹ and W² is NR¹³;

W³ is selected from CR¹R², NR¹⁴, and O;

Z¹ is selected from heteroaryl and heterocycloalkyl;

Z² is selected from aryl, heteroaryl, and heterocycloalkyl;

R⁸ is selected from hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, and optionally substituted heterocycloalkyl;

R¹, R², R¹¹, and R¹² are independently selected from hydrogen, hydroxy, carboxy, sulfonyl, sulfinyl, sulfanyl, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted alkoxy, optionally substituted aryloxy, optionally substituted heteroaryloxy, optionally substituted heterocycloalkyloxy, optionally substituted aminocarbonyloxy, optionally substituted acyloxy, optionally substituted alkoxycarbonyloxy, optionally substituted alkoxycarbonyl, optionally substituted amino, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aminocarbonyl, and optionally substituted aminosulfonyl; or R¹ and R² may optionally be joined together with any intervening atoms to form a group selected from optionally substituted cycloalkyl and optionally substituted heterocycloalkyl;

R¹³ and R¹⁴ are independently selected from hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, and optionally substituted heterocycloalkyl;

for each occurrence, R³, R⁴, R⁵, and R⁶ are independently selected from hydrogen, hydroxy, carboxy, sulfonyl, sulfinyl, sulfanyl, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted alkoxy, optionally substituted aryloxy, optionally substituted heteroaryloxy, optionally substituted heterocycloalkyloxy, optionally substituted aminocarbonyloxy, optionally substituted acyloxy, optionally substituted alkoxycarbonyloxy, optionally substituted acyl, optionally substituted alkoxycarbonyl, optionally substituted amino, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aminocarbonyl, and optionally substituted aminosulfonyl; or R⁵ and R⁶ taken together form an optionally substituted ring selected from optionally substituted cycloalkyl and optionally substituted heterocycloalkyl.

or R¹ and one occurrence of R⁵ may optionally be joined together with any intervening atoms to form a group selected from optionally substituted cycloalkyl and optionally substituted heterocycloalkyl;

or R¹⁴ and one occurrence of R⁵ may optionally be joined together with any intervening atoms to form an optionally substituted heterocycloalkyl ring;

or if W¹ is NR¹³, then R¹³ and R¹⁴ may optionally be joined together with any intervening atoms to form an optionally substituted heterocycloalkyl ring;

or if W¹ is NR¹³, then R¹³ and one occurrence of R⁵ may optionally be joined together with any intervening atoms to form an optionally substituted heterocycloalkyl ring;

R⁷ and R¹⁰ are independently selected from hydrogen, cyano, halo, hydroxy, azido, nitro, carboxy, sulfinyl, sulfanyl, optionally substituted alkoxy, optionally substituted aryloxy, optionally substituted heteroaryloxy, optionally substituted heterocycloalkyloxy, optionally substituted alkoxycarbonyl, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted aryloxy, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted heterocycloalkyl, optionally substituted amino, optionally substituted acyl, optionally substituted alkoxycarbonyl, optionally substituted aminocarbonyl, optionally substituted aminosulfonyl, optionally substituted carbaminodoyl, and optionally substituted alkynyl;

m is selected from 0, 1, 2, and 3;

n is selected from 0, 1, 2, 3, and 4;

p is selected from 0, 1, 2, and 3; and

q is selected from 1, 2, 3, and 4.

In some embodiments, Z¹ is selected from heteroaryl and heterocycloalkyl. In some embodiments, Z¹ is selected from quinolinyl, isoquinolinyl, pyridino[4,3-d]pyridinyl, benzothiazolyl, thiadiazolyl, pyridino[3,4-d]pyridinyl, pyridinyl, pyridino[3,2-d]pyridinyl, 8-hydropyrrolo[1,2-e]pyrimidinyl, isoxazolyl, 8-hydropyrazolo[1,5-a]pyridinyl, pyridino[2,3-d]pyridinyl, benzo[d]isozaolyl, pyrazinyl, thiazolyl, 4-oxo-3-hydroquinazolinyl, 4-hydroimidazo[1,2-a]pyridinyl, 1,3-thiazolo[5,4-b]pyridinyl, oxadiazolyl, benzoxazolyl, quinoxalinyl, thienyl, pyrimidinyl, benzimidazoll, piperidinyl, and pyrazolyl. In some embodiments, Z¹ is selected from isoquinolin-3-yl, benzo[d]thiazol-2-yl, benzo[d]oxazol-2-yl, 1,3,4-thiadiazol-2-yl, pyridin-2-yl, quinolin-2-yl, quinolin-3-yl, thiazol-5-yl, thien-2-yl, and pyrrolo[1,2-c]pyrimidin-3-yl.

In some embodiments, Z² is selected from aryl, heteroaryl, and heterocycloalkyl. In some embodiments, Z² is selected from phenyl, naphthyl, and indanyl. In some embodiments, Z² is phenyl.

In some embodiments, W¹ is CR¹¹R¹².

In some embodiments, R¹¹ and R¹² are each independently selected from hydrogen and optionally substituted lower alkyl.

In some embodiments, R¹¹ and R¹² are each independently selected from hydrogen and lower alkyl.

In some embodiments, R¹¹ and R¹² are both hydrogen.

In some embodiments, W¹ is NR¹³.

In some embodiments, R¹³ is selected from hydrogen and optionally substituted lower alkyl.

In some embodiments, R¹³ is selected from hydrogen and lower alkyl.

In some embodiments, R¹³ is hydrogen.

In some embodiments, W¹ is O.

In some embodiments, W² is CR¹¹R¹².

In some embodiments, R¹¹ and R¹² are each independently selected from hydrogen and optionally substituted lower alkyl.

In some embodiments, R¹¹ and R¹² are each independently selected from hydrogen and lower alkyl.

In some embodiments, R¹¹ and R¹² are both hydrogen.

In some embodiments, W² is NR¹³.

In some embodiments, R¹³ is selected from hydrogen and optionally substituted lower alkyl.

In some embodiments, R¹³ is selected from hydrogen and lower alkyl.

In some embodiments, R¹³ is hydrogen.

In some embodiments, W² is O.

In some embodiments, W¹ is O and W² is NR¹³. In some embodiments, R¹³ is hydrogen.

In some embodiments, W³ is CR¹R².

In some embodiments, R¹ and R² are independently selected from hydrogen and optionally substituted alkyl.

In some embodiments, R¹ and R² are independently selected from hydrogen and optionally substituted lower alkyl.

In some embodiments, R¹ and R² are independently selected from hydrogen and lower alkyl.

In some embodiments, R¹ and R² are independently selected from hydrogen and methyl.

In some embodiments, R¹ and R², together with the carbon to which they are attached, form a group selected from optionally substituted cycloalkyl and optionally substituted heterocycloalkyl.

In some embodiments, R¹ and R², together with the carbon to which they are attached, form a group selected from cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, piperidinyl, and tetrahydropyranyl, any of which is optionally substituted.

In some embodiments, R¹ and R², together with the carbon to which they are attached, form a group selected from piperidine and tetrahydropyran, either of which is optionally substituted with 2-aminoacetyl or 2-(tert-butoxycarbonylamino)acetyl.

In some embodiments, R¹ and R², together with the carbon to which they are attached, form a group selected from tetrahydropyran, 1-(2-(tert-butoxycarbonylamino)acetyl)piperidin-4-yl, and 1-(2-aminoacetyl)piperidin-4-yl.

In some embodiments, W³ is NR¹⁴.

In some embodiments, R¹⁴ is selected from hydrogen and optionally substituted lower alkyl.

In some embodiments, R¹⁴ is selected from hydrogen, lower alkyl, and lower alkyl substituted with one or two groups selected from hydroxy, halo, optionally substituted amino, and optionally substituted alkoxy.

In some embodiments, R¹⁴ is selected from hydrogen, lower alkyl, and lower alkyl substituted with one or two groups selected from hydroxy, optionally substituted amino, and optionally substituted alkoxy.

In some embodiments, R¹⁴ is selected from hydrogen, methyl, ethyl, propyl, and isopropyl, wherein methyl, ethyl, propyl, and isopropyl are optionally substituted with one or two groups selected from hydroxy, optionally substituted amino, and optionally substituted alkoxy.

In some embodiments, R¹⁴ is selected from hydrogen, methyl, ethyl, propyl, and isopropyl, wherein methyl, ethyl, propyl, and isopropyl are optionally substituted with one or two hydroxy groups.

In some embodiments, R¹⁴ is selected from methyl, ethyl, hydroxymethyl, 2-hydroxyethyl, 2,2-difluoroethyl, and isopropyl.

In some embodiments, R¹⁴ is selected from methyl, ethyl, hydroxymethyl, 2-hydroxyethyl, and isopropyl.

In some embodiments, R¹⁴ is selected from methyl and ethyl. In some embodiments, R¹⁴ is methyl.

In some embodiments, R⁸ is selected from hydrogen and optionally substituted lower alkyl.

In some embodiments, R⁸ is selected from hydrogen and lower alkyl.

In some embodiments, R⁸ is selected from hydrogen and methyl.

In some embodiments, R⁸ is hydrogen.

In some embodiments, q is 3.

In some embodiments, q is 2.

In some embodiments, q is 1.

In some embodiments, for each occurrence, each R⁵ is independently selected from hydrogen, optionally substituted lower alkyl, and optionally substituted alkenyl.

In some embodiments, for each occurrence, each R⁵ is independently selected from hydrogen and optionally substituted lower alkyl.

In some embodiments, for each occurrence, each R⁵ is independently selected from hydrogen, lower alkyl, and lower alkyl substituted with one, two, or three groups selected from optionally substituted heterocycloalkyl, optionally substituted heteroaryl, optionally substituted alkoxy, optionally substituted alkoxycarbonyl, hydroxy, optionally substituted amino, optionally substituted aminocarbonyl, acyl, halo, and azido.

In some embodiments, for each occurrence, each R⁵ is independently selected from hydrogen, lower alkyl, and lower alkyl substituted with one, two, or three groups selected from optionally substituted heterocycloalkyl, optionally substituted alkoxy, optionally substituted alkoxycarbonyl, hydroxy, optionally substituted amino, optionally substituted aminocarbonyl, acyl, and azido.

In some embodiments, for each occurrence, each R⁵ is independently selected from hydrogen, lower alkyl, and lower alkyl substituted with one, two, or three groups selected from 4-(lower alkyl)piperazin-1-yl, oxopiperazin-1-yl, morpholino, benzyloxy, benzyloxycarbonyl, methoxycarbonyl, hydroxy, amino, dimethylamino, methoxy(methyl)carbamoyl, acetamido, acetyl, and azido.

In some embodiments, for each occurrence, each R⁵ is independently selected from hydrogen, methyl, ethyl, isopropyl, isobutyl, n-propyl, n-butyl, n-pentyl, isopentyl, and 4-methylpentyl, wherein each of methyl, ethyl, isopropyl, isobutyl, n-propyl, n-butyl, n-pentyl, isopentyl, and 4-methylpentyl is optionally substituted with one, two, or three groups selected from 4-methylpiperazin-1-yl, 3-oxopiperazin-1-yl, morpholino, benzyloxy, benzyloxycarbonyl, methoxycarbonyl, hydroxy, amino, dimethylamino, methoxy(methyl)carbamoyl, acetamido, acetyl, and azido.

In some embodiments, for each occurrence, each R⁵ is independently selected from hydrogen, ethyl, 2-(benzyloxy)-2-oxoethyl, benzyloxymethyl, isobutyl, isopropyl, methyl, 2-hydroxyethyl, 2-methoxy-2-oxoethyl, 3-(benzyloxy)-3-oxopropyl, 3-hydroxypropyl, 3-methoxy-3-oxopropyl, 4-aminobutyl, 4-azidobutyl, 4-hydroxybutyl, 4-methoxy-4-oxobutyl, hydroxymethyl, 2-hydroxy-2-methylpropyl, 4-hydroxy-4-methylpentyl, 3-aminopropyl, (4-methylpiperazin-1-yl)methyl, 2-(3-oxopiperazin-1-yl)ethyl, morpholinoethyl, morpholinomethyl, (3-oxopiperazin-1-yl)methyl, (4-methylpiperazin-1-yl)ethyl, (dimethylamino)methyl, (R)-2-hydroxypropyl, (S)-2-hydroxypropyl, 2-(methoxy(methyl)amino)-2-oxoethyl, 3-(methoxy(methyl)amino)-3-oxopropyl, 3-hydroxy-3-methylbutyl, 3-hydroxybutyl, 4-acetamidobutyl, 4-hydroxypentyl, and 4-oxopentyl.

In some embodiments, for each occurrence, each R⁶ is independently selected from hydrogen and optionally substituted lower alkyl.

In some embodiments, for each occurrence, each R⁶ is independently selected from hydrogen and lower alkyl.

In some embodiments, for each occurrence, R⁶ is hydrogen.

In some embodiments, —(CR⁵R⁶)_(q)— is —CH₂CH(R⁵)— wherein R⁵ is selected from hydrogen, lower alkyl, and lower alkyl substituted with one, two, or three groups selected from 4-(lower alkyl)piperazin-1-yl, oxopiperazin-1-yl, morpholino, benzyloxy, benzyloxycarbonyl, methoxycarbonyl, hydroxy, amino, dimethylamino, methoxy(methyl)carbamoyl, acetamido, acetyl, azido, phosphato (such as —OP(O)(OH)₂), and halo.

In some embodiments, —(CR⁵R⁶)_(q)— is —CH₂CH(R⁵)— wherein R⁵ is lower alkyl substituted with one, two, or three groups selected from hydroxy and phosphato (such as —OP(O)(OH)₂). In some embodiments, —(CR⁵R⁶)_(q)— is —CH₂CH(R⁵)— wherein R⁵ is lower alkyl substituted with —OP(O)(OH)₂ and optionally further substituted with one or two hydroxy groups.

In some embodiments, —(CR⁵R⁶)_(q)— is —CH₂CH(R⁵)— wherein R⁵ is lower alkyl substituted with optionally substituted heteroaryl. In some embodiments, R⁵ is lower alkyl substituted with imidazol-4-yl, imidazol-2-yl, pyridin-2-yl, 1,2,4-oxadiazol-5-yl, isoxazol-5-yl, imidazo[1,5-a]piperazin-3-yl, or 4-hydroimidazo[1,5-a]pyrazin-3-yl, each of which is optionally substituted. In some embodiments, R⁵ is lower alkyl substituted with imidazol-4-yl, imidazol-2-yl, pyridin-2-yl, 1,2,4-oxadiazol-5-yl, isoxazol-5-yl, imidazo[1,5-a]piperazin-3-yl, or 4-hydroimidazo[1,5-a]pyrazin-3-yl, each of which is optionally substituted with a lower alkyl group.

In some embodiments, —(CR⁵R⁶)_(q)— is —CH₂CH(R⁵)— wherein R⁵ is lower alkyl substituted with optionally substitute aminocarbonyl. In some embodiments, R⁵ is lower alkyl substituted with —C(O)NR¹¹R¹² wherein R¹¹ and R¹², together with the nitrogen to which they are bound, form an optionally substituted 5- to 7-membered heterocycloalkyl ring or optionally substituted 8- to 12-membered bicyclic heterocycloalkyl ring, each of which optionally includes an additional heteroatom chosen from oxygen, sulfur, and nitrogen. In some embodiments, R⁵ is lower alkyl substituted with —C(O)NR¹¹ wherein R¹¹ and R¹², together with the nitrogen to which they are bound, form a ring chosen from 4-piperazinyl, 1,4-diazaperhydroepinyl, and 4,5,6,7-tetrahydroimidazo[5,4-c]pyridin-5-yl, each of which is optionally substituted. In some embodiments, R⁵ is lower alkyl substituted with —C(O)NR¹¹R¹² wherein R¹¹ and R¹², together with the nitrogen to which they are bound, form a 4-piperazinyl ring which is optionally substituted. In some embodiments, R⁵ is lower alkyl substituted with —C(O)NR¹¹R¹² wherein R¹¹ and R¹², together with the nitrogen to which they are bound, form a 4-piperazinyl ring which is optionally substituted with one or two groups chosen from lower alkyl, hydroxy substituted lower alkyl, and halo substituted lower alkyl.

In some embodiments, W² is NH, W¹ is O, and W³ is CR¹R².

In some embodiments, W² is NH, W¹ is CH₂, and W³ is NR¹⁴.

In some embodiments, W² is NH, W¹ is O, and W³ is NR¹⁴.

In some embodiments, m is 0.

In some embodiments, m is selected from 1 and 2, and each R⁷ is selected from halo and optionally substituted alkyl.

In some embodiments, R⁷ is selected from halo and optionally substituted lower alkyl.

In some embodiments, R⁷ is selected from halo and lower alkyl.

In some embodiments, each R⁷ is selected from chloro, fluoro, and methyl.

In some embodiments, —(R⁷)_(m), together with Z² to which it is attached, forms a group selected from 2-chlorophenyl, 2-methylphenyl, 2-chloro-4-fluorophenyl, 2-chloro-3-fluorophenyl, 2,3-dichlorophenyl, 2,3-difluorophenyl, 2,4-dichlorophenyl, 2,4-difluorophenyl, and 3-chloro-2-fluorophenyl.

In some embodiments, n is selected from 1 and 2.

In some embodiments, n is 1.

In some embodiments, each R³ and R⁴ is independently selected from hydrogen and optionally substituted lower alkyl.

In some embodiments, each R³ and R⁴ is independently selected from hydrogen, methyl, ethyl, isopropyl, and hydroxymethyl.

In some embodiments, R³ and R⁴ is hydrogen.

In some embodiments, Z¹ is heteroaryl, p is selected from 0, 1, and 2, and R¹⁰ is selected from halo, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted heterocycloalkyl, and optionally substituted aryl.

In some embodiments, Z¹ is heteroaryl, p is selected from 0, 1, and 2, and R¹⁰ is selected from halo, optionally substituted alkyl, optionally substituted alkenyl, and optionally substituted aryl.

In some embodiments, Z¹ is isoquinolinyl, p is 1, and R¹⁰ is halo. In some embodiments, Z¹ is 6-fluoroisoquinolin-3-yl.

In some embodiments, Z¹ is pyridin-2-yl, p is 1, and R¹⁰ is chosen from halo and optionally substituted lower alkyl. In some embodiments, Z¹ is pyridin-2-yl, p is 1, and R¹⁰ is chosen from halo and trifluoromethyl.

In some embodiments, Z¹ is isoxazol-3-yl, p is 1, and R¹⁰ is chosen from optionally substituted phenyl. In some embodiments, Z¹ is isoxazol-3-yl, p is 1, and R¹⁰ is chosen from phenyl and halophenyl.

In some embodiments, Z¹ is isoxazol-5-yl, p is 1, and R¹⁰ is chosen from optionally substituted phenyl. In some embodiments, Z¹ is isoxazol-5-yl, p is 1, and R¹⁰ is chosen from phenyl and halophenyl.

In some embodiments, p is 0 and Z¹ is selected from 2,7-naphthyridinyl, isoquinolinyl, benzo[d]thiazolyl, benzo[d]oxazolyl, 1,3,4-thiadiazolyl, pyridinyl, quinolinyl, thiazolyl, thienyl, and pyrrolo[1,2-c]pyrimidinyl.

In some embodiments, p is 0 and Z¹ is selected from isoquinolinyl, benzo[d]thiazolyl, benzo[d]oxazolyl, 1,3,4-thiadiazolyl, pyridinyl, quinolinyl, thiazolyl, thienyl, and pyrrolo[1,2-c]pyrimidinyl.

In some embodiments, p is 0 and Z¹ is isoquinolin-3-yl. In some embodiments, p is 0 and Z¹ is benzo[d]thiazolyl.

In some embodiments, p is 0 and Z¹ is 2,7-naphthyridin-3-yl.

In some embodiments, Z¹ is selected from isoquinolin-3-yl, isoxazol-3-yl, benzo[d]thiazol-2-yl, benzo[d]oxazol-2-yl, 1,3,4-thiadiazol-2-yl, pyridin-2-yl, quinolin-2-yl, quinolin-3-yl, thiazol-5-yl, thien-2-yl, and pyrrolo[1,2-c]pyrimidin-3-yl, p is selected from 1 and 2, and each R¹⁰ is independently selected from halo, optionally substituted alkyl, optionally substituted alkenyl, and optionally substituted aryl.

In some embodiments, Z¹ is selected from isoquinolin-3-yl, benzo[d]thiazol-2-yl, benzo[d]oxazol-2-yl, 1,3,4-thiadiazol-2-yl, pyridin-2-yl, quinolin-2-yl, quinolin-3-yl, thiazol-5-yl, thien-2-yl, and pyrrolo[1,2-c]pyrimidin-3-yl. p is selected from 1 and 2, and each R¹⁰ is independently selected from halo, optionally substituted alkyl, optionally substituted alkenyl, and optionally substituted aryl.

In some embodiments, R¹⁰ is independently selected from halo, optionally substituted lower alkyl, optionally substituted lower alkenyl, and optionally substituted phenyl.

In some embodiments, R¹⁰ is independently selected from chloro, fluoro, bromo, trifluoromethyl, methyl, ethyl, vinyl, and phenyl.

In some embodiments, Z¹ is isoquinolin-3-yl, p is selected from 1 and 2, and each R¹⁰ is independently selected from halo. In some embodiments, Z¹ is isoquinolin-3-yl, p is selected from 1 and 2, and each R¹⁰ is fluoro. In some embodiments, Z¹ is isoquinolin-3-yl, p is 1, and R¹⁰ is fluoro.

In some embodiments, Z¹ is isoxazol-5-yl, p is 1, and R¹⁰ is selected from optionally substituted phenyl. In some embodiments, Z¹ is isoxazol-5-yl, p is 1, and R¹⁰ is selected from phenyl optionally substituted with one or two halo groups.

In some embodiments, Z¹ is isoxazol-3-yl, p is 1, and R¹⁰ is selected from optionally substituted phenyl. In some embodiments, Z¹ is isoxazol-3-yl, p is 1, and R¹⁰ is selected from phenyl optionally substituted with one or two halo groups.

In some embodiments, Z¹ is 1,3,4-thiadiazol-2-yl, p is 1, and R¹⁰ is selected from optionally substituted phenyl. In some embodiments, Z¹ is isoxazol-3-yl, p is 1, and R¹⁰ is selected from phenyl optionally substituted with one or two halo groups.

In some embodiments, —(R¹⁰)_(p), together with Z¹, forms a group selected from 3-phenylisoxazol-5-yl, 5-phenylisoxazol-3-yl, 6-methylbenzo[d]thiazol-2-yl, 5-ethylpyridin-2-yl, 4-methylbenzo[d]thiazol-2-yl, 5,6-dichlorobenzo[d]thiazol-2-yl, 5,6-difluorobenzo[d]thiazol-2-yl, 5,6-dimethylbenzo[d]thiazol-2-yl, 5-bromopyridin-2-yl, 5-phenyl-1,3,4-thiadiazol-2-yl, 5-vinylpyridin-2-yl, 6-fluoroisoquinolin-3-yl, 5-fluoroisoquinolin-3-yl, 7-fluoroisoquinolin-3-yl, 6-(trifluoromethyl)benzo[d]thiazol-2-yl, 5-phenylpyridin-2-yl, 4-methyl-2-phenylthiazol-5-yl, 5-methylpyridin-2-yl, 5-bromopyridin-2-yl, and 4-methylthiophen-2-yl.

In some embodiments, —(R¹⁰)_(p), together with Z¹, forms a group selected from 6-methylbenzo[d]thiazol-2-yl, 5-ethylpyridin-2-yl, 4-methylbenzo[d]thiazol-2-yl, 5,6-dichlorobenzo[d]thiazol-2-yl, 5,6-difluorobenzo[d]thiazol-2-yl, 5,6-dimethylbenzo[d]thiazol-2-yl, 5-bromopyridin-2-yl, 5-phenyl-1,3,4-thiadiazol-2-yl, 5-vinylpyridin-2-yl, 6-fluoroisoquinolin-3-yl, 5-fluoroisoquinolin-3-yl, 7-fluoroisoquinolin-3-yl, 6-(trifluoromethyl)benzo[d]thiazol-2-yl, 5-phenylpyridin-2-yl, 4-methyl-2-phenylthiazol-5-yl, 5-methylpyridin-2-yl, 5-bromopyridin-2-yl, and 4-methylthiophen-2-yl.

Also provided is at least one chemical entity selected from compounds of Formula II

and pharmaceutically acceptable salts thereof wherein W¹, W², W³, Z¹, R³, R⁴, R⁵, R⁶, R⁷, R⁸, R¹⁰, m, n, p, and q are as described for compounds of Formula I.

Also provided is at least one chemical entity selected from compounds of Formula III

and pharmaceutically acceptable salts thereof wherein Z¹, R³, R⁴, R⁵, R⁶, R⁷, R⁸, R¹⁰, m, and p are as described for compounds of Formula I.

Also provided is at least one chemical entity selected from selected from

Structure Chemical Name

N-[(2-chlorophenyl)methyl](4-{[N-(1- ethyl(4-piperidyl))carbamoyloxy]methyl} (2H-3,4,5,6-tetrahydropyran-4- yl))carboxamide

N-[(2-chlorophenyl)methyl](4-{[N- (4-methyl-2-phenyl(1,3-thiazol-5- yl))carbamoyloxy]methyl}(2H-3,4,5,6- tetrahydropyran-4-yl))carboxamide

{1-(2-aminoacetyl)-4-[(N-(2- thienyl)carbamoyloxy)methyl](4- piperidyl)}-N-[(2- chlorophenyl)methyl]carboxamide

(tert-butoxy)-N-[2-(4-{N-[(2- chlorophenyl)methyl]carbamoyl}-4-{[N- (4-methyl(2-thienyl))carbamoyloxy]methyl} piperidyl)-2-oxoethyl]carboxamide

{[(2-chlorophenyl)methyl]amino}-N- methyl-N-{2-[N-(6-methyl(3-pyridyl)) carbamoyloxy]ethyl}carboxamide

N-(4,5-dimethyl(1,3-thiazol-2-yl))[2-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N- (5-methyl(1,3-thiazol-2-yl))carboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N- (5-methyl(2-pyridyl))carboxamide

{[(2-chlorophenyl)methyl]amino}-N- methyl-N-(2-{N-[6-(trifluoromethyl)(3- pyridyl)]carbamoyloxy}ethyl) carboxamide

{[(2-chlorophenyl)methyl]amino}-N- methyl-N-{2-[N-(5-methylpyrazin-2- yl)carbamoyloxy]ethyl}carboxamide

{[(2-chlorophenyl)methyl]amino}-N- methyl-N-{2-[N-(4-methylbenzothiazol- 2-yl)carbamoyloxy]ethyl}carboxamide

{[(2-chlorophenyl)methyl]amino}-N- methyl-N-{2-[N-(5-methyl(1,3,4- thiadiazol-2-yl))carbamoyloxy]ethyl} carboxamide

{[(2-chlorophenyl)methyl]amino}-N- methyl-N-{2- [N-(5-phenyl(1,3,4-thiadiazol-2- yl))carbamoyloxy]ethyl}carboxamide

{[(2-chlorophenyl)methyl]amino}- N-{2-[N-(5-ethyl(1,3,4-thiadiazol-2- yl))carbamoyloxy]ethyl}- N-methylcarboxamide

{[(2-chlorophenyl)methyl]amino}-N- methyl-N-(2-{N-[5- (trifluoromethyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}ethyl)carboxamide

{[(2-chlorophenyl)methyl]amino}-N- methyl-N-{2-[N-(5-methylisoxazol-3- yl)carbamoyloxy]ethyl}carboxamide

{[(2-chlorophenyl)methyl]amino}-N- methyl-N-{2-[N-(3-methylisoxazol-5- yl)carbamoyloxy]ethyl}carboxamide

N-{2-[N-(5-bromopyrimidin-2- yl)carbamoyloxy]ethyl}{[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

N-{2-[N-(5-bromopyrazin-2- yl)carbamoyloxy]ethyl}{[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

[2-({[(2-chlorophenyl)methyl] amino}-N-methylcarbonylamino) ethoxy]-N-(5-cyano(2-pyridyl)) carboxamide

[2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)ethoxy]-N-[5- (trifluoromethyl)(2-pyridyl)] carboxamide

[2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)ethoxy]-N-(5- fluoro(2-pyridyl))carboxamide

N-(5-bromo(2-pyridyl))[2-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy] carboxamide

[2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)ethoxy]-N- (4-methyl(2-pyridyl))carboxamide

[2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)ethoxy]-N-(2- pyridyl)carboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-(5- phenyl(2-pyridyl))carboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-(5- vinyl(2-pyridyl))carboxamide

[2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)ethoxy]-N- (5-ethyl(2-pyridyl))carboxamide

N-(5-ethyl(2-pyridyl))2-{N- methyl[benzylamino]carbonylamino} ethoxy)carboxamide

N-[2-(N-benzothiazol-2- ylcarbamoyloxy)ethyl]{[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

{[(2-chlorophenyl)methyl]amino}-N- methyl-N-{2-[N-(6-methylbenzothiazol- 2-yl)carbamoyloxy]ethyl}carboxamide

methyl 6-{[2-({[(2-chlorophenyl)methyl] amino}-N-methylcarbonylamino)ethoxy] carbonylamino}pyridine-3-carboxylate

{[(2-chlorophenyl)methyl]amino}-N- methyl-N-{2-[N-(1-phenylpyrazol-3- yl)carbamoyloxy]ethyl}carboxamide

[2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)ethoxy]-N- (5-phenyl(1,3,4-oxadiazol-2-yl)) carboxamide

N-[5-(tert-butyl)isoxazol-3-yl][2-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carboxamide

N-benzo[d]isoxazol-3-yl[2-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy] carboxamide

N-benzimidazol-2-yl[2-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy] carboxamide

6-{[2-({[(2-chlorophenyl)methyl] amino}-N-methylcarbonylamino) ethoxy]carbonylamino} pyridine-3-carboxamide

{[(2-chlorophenyl)methyl]amino}-N- (2-{N-[5-(hydroxymethyl)(2-pyridyl)] carbamoyloxy}ethyl)-N- methylcarboxamide

N-{2-[N-(5-acetyl(2- pyridyl))carbamoyloxy]ethyl}{[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

{[(2-chlorophenyl)methyl]amino}-N- (2-{N-[5-(hydroxyethyl)(2-pyridyl)] carbamoyloxy}ethyl)-N- methylcarboxamide

{[(2-chlorophenyl)methyl]amino}-N- (2-{N-[5-(1-hydroxy-isopropyl)(2- pyridyl)]carbamoyloxy}ethyl)-N- methylcarboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-(3- isoquinolyl)carboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-(2- quinolyl)carboxamide

(1-(2-aminoacetyl)-4-{[N-(5-bromo(2- pyridyl))carbamoyloxy]methyl}(4- piperidyl))-N-[(2,3-dichlorophenyl) methyl]carboxamide

{[(2-chlorophenyl)methyl]amino}-N- methyl-N-[2-(N-(6-quinolyl) carbamoyloxy) ethyl]carboxamide

N-[2-(N-benzothiazol-6- ylcarbamoyloxy)ethyl]{[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

{1-(2-aminoacetyl)-4-[(N-(2- quinolyl)carbamoyloxy)methyl](4- piperidyl)}-N-[(2-chlorophenyl) methyl]carboxamide

(1-(2-aminoacetyl)-4-{[N-(4- methylbenzothiazol-2- yl)carbamoyloxy]methyl} (4-piperidyl))-N-[(2- chlorophenyl)methyl]carboxamide

(1-(2-aminoacetyl)-4-{[N-(5- phenyl(2-pyridyl))carbamoyloxy] methyl}(4-piperidyl))-N- [(2-chlorophenyl)methyl]carboxamide

(1-(2-aminoacetyl)-4-{[N-(5-methyl(2- pyridyl))carbamoyloxy]methyl}(4- piperidyl))-N-[(2-chlorophenyl) methyl]carboxamide

(1-(2-aminoacetyl)-4-{[N-(5-phenyl(1,3,4- thiadiazol-2-yl))carbamoyloxy]methyl}(4- piperidyl))-N-[(2- chlorophenyl)methyl]carboxamide

{1-(2-aminoacetyl)-4-[(N-(3- isoquinolyl)carbamoyloxy)methyl](4- piperidyl)}-N-[(2-chlorophenyl) methyl]carboxamide

(1-(2-aminoacetyl)-4-{[N-(6- methylbenzothiazol-2- yl)carbamoyloxy]methyl}(4-piperidyl))- N-[(2-chlorophenyl)methyl] carboxamide

[1-(2-aminoacetyl)-4-({N-[6- (trifluoromethyl)benzothiazol-2- yl]carbamoyloxy}methyl)(4-piperidyl)]- N-[(2-chlorophenyl)methyl] carboxamide

N-[2-(N-benzothiazol-2- ylcarbamoyloxy)ethyl]{[(2- chlorophenyl)methyl]amino}-N-(2- hydroxyethyl)carboxamide

[(2S)-2-({[(2-chlorophenyl) methyl]amino}-N- methylcarbonylamino)butoxy]-N- (3-isoquinolyl)carboxamide

[(2S)-2-({[(2-chlorophenyl)methyl] amino}-N-methylcarbonylamino) butoxy]-N-(6-methylbenzothiazol-2-yl) carboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N- quinoxalin-2-ylcarboxamide

N-(5,6-dimethylbenzothiazol-2-yl)[2-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-[6- (methylsulfonyl)benzothiazol-2-yl] carboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-[6- (trifluoromethoxy)benzothiazol-2-yl] carboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-[6- (trifluoromethyl)benzothiazol-2-yl] carboxamide

ethyl 2-{[2-({[(2-chlorophenyl)methyl] amino}-N-methylcarbonylamino) ethoxy]carbonylamino} benzothiazole-6-carboxylate

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-(6- methoxybenzothiazol-2-yl) carboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-(4- methoxybenzothiazol-2-yl)carboxamide

N-(5,6-dichlorobenzothiazol-2-yl)[2-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carboxamide

[(2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-(1,3- thiazolo[5,4-b]pyridin-2-yl)carboxamide

2-{[2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)ethoxy] carbonylamino} benzothiazole-6-carboxamide

[2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)ethoxy]- N-(5-(3-pyridyl)(1,3,4-thiadiazol-2- yl))carboxamide

[2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)ethoxy]- N-(5-(4-pyridyl)(1,3,4-thiadiazol-2- yl))carboxamide

[(2S)-2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)-3-methylbutoxy]- N-(3-isoquinolyl)carboxamide

[(2S)-2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)-3- methylbutoxy]-N-(6- methylbenzothiazol-2-yl)carboxamide

[(2S)-2-({[(2-chlorophenyl)methyl] amino}-N-methylcarbonylamino)- 4-methylpentyloxy]- N-(3-isoquinolyl)carboxamide

[(2S)-2-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)-4- methylpentyloxy]- N-(6-methylbenzothiazol-2- yl)carboxamide

{[(2-chlorophenyl)methyl]amino}-N- [2-(3-diazo-3-azaprop-3-enyloxy)ethyl]- N-[2-(N-(3-isoquinolyl)carbamoyloxy) ethyl]carboxamide

N-[2-(2-aminoethoxy)ethyl]{[(2- chlorophenyl)methyl]amino}-N-[2-(N-(3- isoquinolyl)carbamoyloxy)ethyl] carboxamide

{[(2-chlorophenyl)methyl]amino}-N-[2-(N- (3-isoquinolyl)carbamoyloxy)ethyl]-N-{2- [2-(trimethylamino)ethoxy]ethyl} carboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-(4,5,6,7- tetrahydrobenzothiazol-2-yl)carboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-(4- hydroxy(2-quinolyl))carboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-(3- quinolyl)carboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N- (6-methyl-4-oxo(3- hydroquinazolin-2-yl))carboxamide

phenylmethyl (3S)-3-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)-4-(N-(3- isoquinolyl)carbamoyloxy)butanoate

phenylmethyl (3S)-3-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6- methylbenzothiazol-2-yl)carbamoyloxy] butanoate

[(2S)-2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)-4-hydroxybutoxy]- N-(3-isoquinolyl)carboxamide

methyl (3S)-3-({[(2-chlorophenyl)methyl] amino}-N-methylcarbonylamino)-4-(N-(3- isoquinolyl)carbamoyloxy)butanoate

{[(2-chlorophenyl)methyl]amino}-N-[2-(2- hydroxyethoxy)ethyl]-N-[2-(N-(3- isoquinolyl)carbamoyloxy)ethyl] carboxamide

N-{2-[2-(dimethylamino)ethoxy]ethyl}{[(2- chlorophenyl)methyl]amino}-N-[2-(N-(3- isoquinolyl)carbamoyloxy)ethyl] carboxamide

{[(2-chlorophenyl)methyl]amino}-N-[2-(N- (3-isoquinolyl)carbamoyloxy)ethyl]-N-{2- [2-(methylamino)ethoxy]ethyl} carboxamide

4-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)-N-(3- isoquinolyl)butanamide

3-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)-N-(3- isoquinolyl)propanamide

phenylmethyl (4S)-4-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoate

methyl (4S)-4-({[(2-chlorophenyl)methyl] amino}-N-methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoate

[(2R)-2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)propoxy]-N-(3- isoquinolyl)carboxamide

{[(2-chlorophenyl)methyl]methylamino}- N-[2-(N-(3-isoquinolyl)carbamoyloxy)ethyl]- N-methylcarboxamide

[2-(N-((2R)-2-amino-3-hydroxypropyl){[(2- chlorophenyl)methyl]amino}carbonylamino) ethoxy]-N-(3-isoquinolyl)carboxamide

[(2S)-2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)propoxy]-N-(3- isoquinolyl)carboxamide

[(2S)-2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)-5- hydroxypentyloxy]-N-(3- isoquinolyl)carboxamide

N-{(1S)-2-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]ethyl} {[(2-chlorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-1-[(N-(3-isoquinolyl) carbamoyloxy)methyl]propyl}-N- methyl{[(2-methylphenyl) methyl]amino}carboxamide

N-benzoxazol-2-yl[2-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carboxamide

N-(5,6-difluorobenzothiazol-2-yl)[2-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carboxamide

methyl (5S)-5-({[(2-chlorophenyl) methyl]amino}- N-methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy)hexanoate

(5S)-5-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy)hexanoic acid

N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]pentyl} {[(2-chlorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-6-diazo-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]- 6-azahex-6-enyl} {[(2-chlorophenyl)methyl]amino}- N-methylcarboxamide

N-{(1S)-5-amino-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]pentyl} {[(2-chlorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-2-(N-(3- isoquinolyl)carbamoyloxy)-1- [(phenylmethoxy)methyl]ethyl}{[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-2-(N-(3- isoquinolyl)carbamoyloxy)-1- [(phenylmethoxy)methyl]ethyl}-N- methyl[benzylamino]carboxamide

(3S)-3-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)-4-(N-(3- isoquinolyl)carbamoyloxy)butanoic acid

[(2R)-2-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)-6- hydroxyhexyloxy]-N- (3-isoquinolyl)carboxamide

N-{(1S)-3-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-3- methylbutyl}{[(2- chlorophenyl)methyl]amino)- N-methylcarboxamide

(3S)-3-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)-4-(N-(3- isoquinolyl)carbamoyloxy)-N-methoxy-N- methylbutanamide

N-{(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy) methyl]-3-morpholin-4-ylpropyl} {[(2-chlorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2-chlorophenyl)methyl] amino}-N-methylcarboxamide

N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2-fluorophenyl)methyl] amino}-N-methylcarboxamide

N-{(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy) methyl]-3-(4-methylpiperazinyl) propyl}{[(2-chlorophenyl)methyl] amino}-N-methylcarboxamide

N-{(1S)-3-(4-acetylpiperazinyl)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl] propyl}{[(2-chlorophenyl)methyl] amino}-N-methylcarboxamide

ethyl 4-[(3S)-3-({[(2-chlorophenyl) methyl]amino}-N-methylcarbonyl- amino)-4-(N-(3-isoquinolyl)carbamoyloxy) butyl]piperazinecarboxylate

N-{(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy) methyl]-3-[4-(methylsulfonyl) piperazinyl]propyl}{[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

methyl (5S)-5-({[(2-chloro-4- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy)hexanoate

methyl (5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy)hexanoate

N-{(1S,3S)-3-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl} {[(2-chlorophenyl)methyl]amino}- N-methylcarboxamide

N-{(1S,3R)-3-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl} {[(2-chlorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-4-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-4- methylpentyl}{[(2-chlorophenyl)methyl] amino}-N-methylcarboxamide

N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]pentyl} {[(2-chloro-4-fluorophenyl)methyl] amino}-N-methylcarboxamide

N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2-chloro-4- fluorophenyl)methyl]amino}- N-methylcarboxamide

N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]pentyl} {[(2-chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide

[(2S)-5-amino-2-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)pentyloxy]-N-(3- isoquinolyl)carboxamide

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy)hexanoate

methyl (5S)-5-({[(2,3- dichlorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy)hexanoate

methyl (5S)-5-({[(3-chloro-2- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy)hexanoate

N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]pentyl} {[(2,3-difluorophenyl)methyl] amino}-N-methylcarboxamide

N-{(1S)-4-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]pentyl} {[(2-chlorophenyl)methyl]amino}-N- methylcarboxamide

(5S)-5-({[(2-chlorophenyl)methyl] amino}-N-methylcarbonylamino)- 6-(N-(3-isoquinolyl)carbamoyloxy)- N-methoxy-N- methylhexanamide

N-{(1S)-1-[(N-3-isoquinolyl)carbamoyloxy) methyl]-5-oxohexyl}{[(2-chlorophenyl) methyl]amino}-N-methylcarboxamide

N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]hexyl} {[(2-chlorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]pentyl} {[(2,3-dichlorophenyl)methyl]amino}- N-methylcarboxamide

N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2,3- dichlorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2,3-difluorophenyl) methyl]amino}-N-methylcarboxamide

N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(3-chloro-2- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2,4-difluorophenyl) methyl]amino}-N-methylcarboxamide

N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2,4- dichlorophenyl)methyl]amino}-N- methylcarboxamide

[(2S)-2-({[(2-chlorophenyl)methyl] amino}-N-methylcarbonylamino)-4- hydroxy-4-methylpentyloxy]-N- (5,6-difluorobenzothiazol- 2-yl)carboxamide

N-{(1S)-3-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-3- methylbutyl}{[(2-chloro-4- fluorophenyl)methyl]amino}- N-methylcarboxamide

(3S)-4-[N-(5,6-difluorobenzothiazol-2- yl)carbamoyloxy]-3-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)butanoic acid

methyl (3S)-4-[N-(5,6- difluorobenzothiazol-2- yl)carbamoyloxy]-3-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)butanoate

N-[(5S)-5-({[(2- chlorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy)hexyl] acetamide

{[(2-chlorophenyl)methyl]amino}-N- [2-(N-(4-hydroimidazo[1,2-a]pyridin-2- yl)carbamoyloxy)ethyl]-N- methylcarboxamide

N-((1S)-1-{[N-(5,6-difluorobenzothiazol-2- yl)carbamoyloxy]methyl}-3-hydroxy-3- methylbutyl){[(2-chloro-4- fluorophenyl)methyl]amino}-N- methylcarboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-(8- hydropyrazolo[1,5-a]pyridin-2-yl) carboxamide

N-[(5S)-5-({[(2-chlorophenyl) methyl]amino}-N- methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy)hexyl]- 2-diazo-3,3,3-trifluoropropanamide

N-((1S)-1-{[N-(5,6-difluorobenzothiazol- 2-yl)carbamoyloxy]methyl}-3-hydroxy-3- methylbutyl){[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

N-((1S)-1-{[N-(5,6-difluorobenzothiazol-2- yl)carbamoyloxy]methyl}-3-hydroxy-3- methylbutyl){[(3-chloro-2- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1R)-2-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-2- methylpropyl}{[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

methyl (2R)-2-({[(2-chlorophenyl)methyl] amino}-N-methylcarbonylamino)-3-(N-(3- isoquinolyl)carbamoyloxy)propanoate

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-3- hydroxy-3-methylbutyl){[(2-chloro-4- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}- 3-hydroxy-3-methylbutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-3- hydroxy-3-methylbutyl){[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-3-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-3- methylbutyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-(8- hydropyrrolo[1,2-e]pyrimidin-3-yl) carboxamide

N-{(1S)-2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-1-[(3- oxopiperazinyl)methyl]ethyl}{[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-1-[(4- methylpiperazinyl)methyl]ethyl}{[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

N-[(1S)-2-(N-(3-isoquinolyl) carbamoyloxy)-1- (morpholin-4-ylmethyl)ethyl]{[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

[(2S)-2-({[(2-chlorophenyl) methyl]amino}-N- methylcarbonylamino)-3-(4-methyl-3- oxopiperazinyl)propoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide

[(2S)-2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)-4-hydroxy-3,4- dimethylpentyloxy]-N-(6-fluoro(3- isoquinolyl))carboxamide

[(2S)-2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)-4-hydroxy-3,4- dimethylpentyloxy]-N-(6-fluoro(3- isoquinolyl))carboxamide

N-{(1S)-1-[(dimethylamino)methyl]-2- [N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}{[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

[((2S)-1-{N-[(2-chloro-4- fluorophenyl)methyl] carbamoyl}pyrrolidin- 2-yl)methoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-hydroxy-4- methylpentyloxy]-N-(5-fluoro(3- isoquinolyl))carboxamide

[(2S)-2-({[(2-chloro-4- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-hydroxy-4- methylpentyloxy]-N-(5-fluoro(3- isoquinolyl))carboxamide

[(2S)-2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)-4-hydroxy-4- methylpentyloxy]-N-(5-fluoro(3- isoquinolyl))carboxamide

N-{(1S)-1-[(N-(3-isoquinolyl) carbamoyloxy)methyl]-3-(4-methyl-3- oxopiperazinyl)propyl}{[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-1-[(N-(3-isoquinolyl) carbamoyloxy)methyl]-3-(3- oxopiperazinyl)propyl}{[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-hydroxy-4- methylpentyloxy]-N-(7-fluoro(3- isoquinolyl))carboxamide

[(2S)-2-({[(2-chloro-4- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-hydroxy-4- methylpentyloxy]-N-(7-fluoro(3- isoquinolyl))carboxamide

[(2S)-2-({[(2-chlorophenyl) methyl]amino}-N- methylcarbonylamino)-4-hydroxy-4- methylpentyloxy}-N-(7-fluoro(3- isoquinolyl))carboxamide

{[(2-chloro-3-fluorophenyl) methyl]amino}-N- ethyl-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl} carboxamide

{[(2-chloro-3-fluorophenyl) methyl]amino}- N-{2-[N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}- N-(methylethyl)carboxamide

{[(2-chloro-4-fluorophenyl) methyl]amino}-N- ethyl-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl} carboxamide

{[(2-chloro-4-fluorophenyl) methyl]amino}- N-{2-[N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}- N-(methylethyl)carboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}- 3-hydroxy-3-methylbutyl){[(2- chloro-4-fluorophenyl)methyl] amino}-N-(methylethyl)carboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}- 3-hydroxy-3-methylbutyl){[(2- chlorophenyl)methyl]amino}-N- (methylethyl)carboxamide

[((2S)-1-{N-[(2-chloro-4- fluorophenyl)methyl]carbamoyl} pyrrolidin-2-yl)methoxy]-N-(8- hydropyrrolo[1,2-e]pyrimidin-3- yl)carboxamide

[2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)ethoxy]- N-pyridino[4,3- d]pyridin-3-ylcarboxamide

[((2S)-1-{N-[(2-chloro-3- fluorophenyl)methyl]carbamoyl} pyrrolidin-2- yl)methoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide

{[(2-chloro-3-fluorophenyl)methyl] amino}-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}- N-(2-hydroxy-2-methylpropyl) carboxamide

{[(2-chloro-3-fluorophenyl) methyl]amino}- N-{2-[N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}- N-(2,2,2-trifluoroethyl)carboxamide

{[(2-chloro-3-methoxyphenyl)methyl] amino}-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-N- methylcarboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}- 3-hydroxy-3-methylbutyl){[(2- chlorophenyl)methyl]amino}-N- ethylcarboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}- 3-hydroxy-3-methylbutyl){[(2-chloro- 4-fluorophenyl)methyl]amino}-N- ethylcarboxamide

N-((1S)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl} butyl){[(2-chloro-4-fluorophenyl) methyl]amino}-N- methylcarboxamide

N-((1S)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl} butyl){[(2-bromophenyl)methyl]amino}- N-methylcarboxamide

N-(2-aminoethyl)(4-{N-[(2-chlorophenyl) methyl]carbamoyl}-4-{[N-(6- fluoro(3-isoquinolyl))carbamoyloxy] methyl}piperidyl)carboxamide

(tert-butoxy)-N-[2-(4-{N-[(2- bromophenyl)methyl]carbamoyl}-4-{[N- (4-ethylphenyl)carbamoyloxy]methyl} piperidyl)-2-oxoethyl}-N- methylcarboxamide

[(4-{N-[(2-bromophenyl)methyl] carbamoyl}-1-[2-(methylamino)acetyl](4- piperidyl))methoxy]-N-(4- ethylphenyl)carboxamide

N-(2,2-difluoroethyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-{2- [N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}carboxamide

{[(2-chloro-3-fluorophenyl) methyl]amino}-N-{2- [N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}- N-(3,3,3-trifluoropropyl)carboxamide

[((2S,4R)-1-{N-[(2-chloro-3- fluorophenyl)methyl]carbamoyl}-4- hydroxypyrrolidin-2-yl)methoxy]- N-(6-fluoro(3-isoquinolyl))carboxamide

[((2S)-1-{N-[(2-chloro-3- fluorophenyl)methyl]carbamoyl} pyrrolidin-2-yl)methoxy]-N- pyridino[4,3-d]pyridin-3- ylcarboxamide

{[(2-chloro-3-hydroxyphenyl) methyl]amino}-N-{2- [N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}- N-methylcarboxamide

(2-{1-[(2-chloro-4-fluorophenyl) methyl]-3-methyl- 2-oxopyrrolidin-3-yl}ethoxy)-N- (6-fluoro(3- isoquinolyl))carboxamide

N-((1S)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}butyl){[(2- chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

((5S,3R)-1-{N-[(2-chloro-3- fluorophenyl)methyl]carbamoyl}-5- (hydroxymethyl)pyrrolidin-3-yloxy)- N-(6-fluoro(3- isoquinolyl))carboxamide

{[((2S)-1-{N-[(2-chloro-3- fluorophenyl)methyl]carbamoyl} pyrrolidin-2- yl)methyl]amino}-N-(6-fluoro(3- isoquinolyl))carboxamide

methyl 2-chloro-3-{[(N-{2-[N-(6- fluoro(3-isoquinolyl))carbamoyloxy] ethyl}-N-methylcarbamoyl) amino]methyl}benzoate

4-amino-N-[(2-chloro-4-fluorophenyl) methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-2- methylbutanamide

N-((1S)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}butyl){[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-4-[(2,2-difluoroethyl) amino]-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}butyl){[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

[((2S,4R)-4-amino-1-{N-[(2-chloro- 3-fluorophenyl)methyl]carbamoyl} pyrrolidin-2- yl)methoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide

N-((5S,3R)-1-{N-[(2-chloro-3- fluorophenyl)methyl]carbamoyl}- 5-{[N-(6-fluoro(3-isoquinolyl)) carbamoyloxy}methyl} pyrrolidin-3-yl)-2-[(tert-butoxy) carbonylamino]acetamide

N-((5S,3R)-1-{N-[(2-chloro-3- fluorophenyl)methyl]carbamoyl}- 5-{[N-(6-fluoro(3-isoquinolyl)) carbamoyloxy] methyl}pyrrolidin-3-yl)-2- aminoacetamide

[((2S)-1-{N-[(2-chloro-3- fluorophenyl)methyl]carbamoyl}azetidin- 2-yl)methoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}but-3-enyl) {[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}-3,4- dihydroxybutyl){[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

N-((1S)-4-[(tert-butoxy) carbonylamino]-1-{[N-(6- fluoro(3-isoquinolyl))carbamoyloxy] methyl}butyl){[(2-chloro-3- fluorophenyl)methyl] amino}-N-methylcarboxamide

N-{(1S)-4-amino-1-[(N-(3- isoquinolyl)carbamoyloxy) methyl]butyl}{[(2- chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

N-{(1S)-4-amino-1-[(N-(3- isoquinolyl)carbamoyloxy) methyl]butyl}{[(2- chloro-4-fluorophenyl) methyl]amino}-N- methylcarboxamide

N-{(1S)-4-amino-1-[(N-(3- isoquinolyl)carbamoyloxy) methyl]butyl}{[(2,3- dichlorophenyl)methyl]amino}- N-methylcarboxamide

({[2-chloro-3- (hydroxymethyl)phenyl] methyl}amino)-N-{2-[N- (6-fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}-N- methylcarboxamide

N-[(2-chloro-3-fluorophenyl) methyl]-4-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]-2,2- dimethylbutanamide

N-[(2-chloro-3-fluorophenyl) methyl]-2-{2-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}-2- methylpent-4-enamide

N-[(2-chloro-3-fluorophenyl) methyl]-2-{2-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}-4,5- dihydroxy-2-methylpentanamide

N-[(2-chloro-3-fluorophenyl) methyl]-2-{2-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}-5- hydroxy-2-methylpentanamide

{[(2,5-dichlorophenyl)methyl] amino}-N-{2-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}-N- methylcarboxamide

{[(5-chloro-2-fluorophenyl) methyl]amino}-N-{2- [N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}- N-methylcarboxamide

methyl (4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]pentanoate

ethyl (4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanoate

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-N-methoxy-N- methylpentanamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-4-[(2- fluoroethyl)amino]butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-4-[(2,2-difluoroethyl)amino]-1- {[N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]methyl}butyl){[(2- chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-4- [(2,2,2-trifluoroethyl)amino]butyl) {[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-4-(3,3-difluoroazetidinyl)-1-{[N-(6- fluoro(3-isoquinolyl))carbamoyloxy] methyl}butyl){[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

N-((1S)-4-(3,3-difluoropyrrolidinyl)-1-{[N- (6-fluoro(3-isoquinolyl))carbamoyloxy] methyl}butyl){[(2- chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-4- hydroxybutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(2-chloro-3-fluorophenyl)methyl]-4-[N- (6-fluoro(3-isoquinolyl))carbamoyloxy]-2- methylbutanamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-5- hydroxypentyl){[(2-chlorophenyl) methyl]amino}- N-methylcarboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-5- hydroxypentyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S,3S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}- 3,4-dihydroxybutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S,3R)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-3,4- dihydroxybutyl){[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

4-{2-[(tert-butoxy) carbonylamino]acetylamino}-N- [(2-chloro-3-fluorophenyl) methyl]-2-{2-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}-2- methylbutanamide

4-(2-aminoacetylamino)-N-[(2-chloro-3- fluorophenyl)methyl]-2-{2- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-2- methylbutanamide

5-amino-N-[(2-chloro-3- fluorophenyl)methyl]-2- {2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-2- methylpentanamide

N-[(2-chloro-3-fluorophenyl) methyl]-2-{2-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}-6- hydroxy-2-methylhexanamide

5-(2-aminoacetylamino)-N- [(2-chloro-3- fluorophenyl)methyl]-2-{2- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}- 2-methylpentanamide

N-((1S)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-3- hydroxybutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{2-[N-(5-bromo-4-methyl(2- pyridyl))carbamoyloxy]ethyl} {[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

{[(2-chloro-3-fluorophenyl) methyl]amino}-N-{2- [N-(5-fluoro-4-methyl(2- pyridyl))carbamoyloxy]ethyl}-N- methylcarboxamide

{[(2-chlorophenyl)methyl]amino}- N-{2-[N-(5- fluoro-4-methyl(2-pyridyl)) carbamoyloxy]ethyl}- N-methylcarboxamide

N-((1S)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}pentyl){[(2- chloro-3-fluorophenyl)methyl] amino}-N- methylcarboxamide

N-[(2-chloro-3-fluorophenyl) methyl]-2-{2-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}-2- methylpentanamide

(2S)-N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]pentyl]-2-amino-3- hydroxypropanamide

(2R)-N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]- 2-amino-3-hydroxypropanamide

N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]-2- aminoacetamide

N-((1S)-4-amino-5,5-difluoro-1- {[N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]methyl}pentyl){[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

N-[(2-chloro-3-fluorophenyl)methyl]-2- {2-[N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}-4- hydroxy-2-methylbutanamide

2-({2-[(tert- butoxy)carbonylamino] acetylamino}methyl)-N-[(2- chloro-3-fluorophenyl)methyl]- 4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-2- methylbutanamide

2-[(2-aminoacetylamino)methyl]- N-[(2-chloro-3- fluorophenyl)methyl]-4- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-2- methylbutanamide

{[(2-chloro-5-fluorophenyl) methyl]amino}-N-{2- [N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}- N-methylcarboxamide

2-{2-[(tert-butoxy) carbonylamino]ethyl}-N-[(2- chloro-3-fluorophenyl) methyl]-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-2- methylbutanamide

4-amino-N-[(2-chloro-3-fluorophenyl) methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-2- methylbutanamide

N-[(2-chloro-3-fluorophenyl)methyl]- 2-{2-[N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}-4-(2- hydroxyacetylamino)-2- methylbutanamide

4-{(2S)-2-[(tert-butoxy)carbonylamino]-3- hydroxypropanoylamino}-N-[(2-chloro-3- fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-2- methylbutanamide

4-((2S)-2-amino-3- hydroxypropanoylamino)-N-[(2- chloro-3-fluorophenyl)methyl]-2- {2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}- 2-methylbutanamide

4-(2,3-dihydroxypropanoylamino)-N- [(2-chloro-3-fluorophenyl)methyl]- 2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-2- methylbutanamide

6-amino-N-[(2-chloro-3- fluorophenyl)methyl]-2- {2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}- 2-methylhexanamide

[((2R,3R)-1-{N-[(2-chloro-3- fluorophenyl)methyl]carbamoyl}-3- hydroxypyrrolidin-2-yl)methoxy]-N- (6-fluoro(3-isoquinolyl))carboxamide

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-2- hydroxypentyl dimethyl phosphate

N-((1S,3S)-1-{[N-(6-fluoro-2-hydroxy(3- isoquinolyl))carbamoyloxy]methyl}-3,4- dihydroxybutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S,3R)-1-[N-(6-fluoro-2-hydroxy(3- isoquinolyl))carbamoyloxy]methyl}-3,4- dihydroxybutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[2-[N-(5-chloro(2- pyridyl))carbamoyloxy]ethyl}{[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

({(4S)-6-(aminomethyl)-1-[(2-chloro-3- fluorophenyl)methyl]- 6-fluoro-3-methyl-2-oxo(1,3- diazaperhydroin-4-yl)}methoxy)- N-(6-fluoro(3- isoquinolyl))carboxamide

N-((1S)-4-amino-5,5-difluoro- 1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}pentyl){[(2- chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide

N-((1S)-5,5-difluoro-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-4- [(phenylmethoxy)carbonylamino]pentyl) {[(2-chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-2- hydroxypentyl hydrogen methyl phosphate

N-((1S)-3,4-diamino-1- {[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl} butyl){[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

6-(2-aminoacetylamino)-N-[(2-chloro-3- fluorophenyl)methyl]-2-{2-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}-2- methylhexanamide

N-[(2-chloro-3-fluorophenyl)methyl]- 2-{2-[N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}-5,6- dihydroxy-2-methylhexanamide

N-((1S,3R)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-3- hydroxybutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S,3S)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-3- hydroxybutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

(4S)-4-({[(2-chloro-3-fluorophenyl) methyl]amino}- N-methylcarbonylamino)-5-[N-(6- fluoro(3-isoquinolyl))carbamoyloxy]- 2-hydroxypentyl dihydrogen phosphate

2-{2-[(2,2-difluoroethyl) amino]ethyl}-N-[(2- chloro-3-fluorophenyl)methyl]-4- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-2- methylbutanamide

{[(2-chloro-3-fluorophenyl) methyl]amino}- N-{2-[N-(5-cyano-4-methyl(2- pyridyl))carbamoyloxy]ethyl}-N- methylcarboxamide

N-{2-[N-(4,5-dimethy(2- pyridyl))carbamoyloxy]ethyl} {[(2-chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide

N-{2-[N-(4,5-dimethyl(2- pyridyl))carbamoyloxy]ethyl}{[(2- chlorophenyl)methyl]amino}-N- methylcarboxamide

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl] amino}-N-methylcarbonylamino)-5- [N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]- 2-hydroxypentyl 2- (dimethylamino)acetate

(3S)-N-(2,3-dihydroxypropyl)- 3-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] butanamide

(3S)-N-{2-[(tert-butoxy) carbonylamino]ethyl}-3- ({[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarbonylamino)-4- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] butanamide

tert-butyl 4-[(3S)-3-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] butanoylamino] piperidinecarboxylate

tert-butyl 4-[(3S)-3-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]butanoyl] piperazinecarboxylate

(3S)-N-(2-aminoethyl)-3-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butanamide

(3S)-3-({[(2-chloro-3-fluorophenyl) methyl]amino}-N-methylcarbonylamino)- 4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-N-(4- piperidyl)butanamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-oxo-4- piperazinylbutoxy]- N-(6-fluoro(3-isoquinolyl))carboxamide

[((2S,3S)-3-amino-1-{N-[(2-chloro-3- fluorophenyl)methyl] carbamoyl}pyrrolidin- 2-yl)methoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide

[((2S,3S)-1-{N-[(2-chloro-3- fluorophenyl)methyl]carbamoyl}-3- (diazoazamvinyl)pyrrolidin-2- yl)methoxy]-N- (6-fluoro(3-isoquinolyl))carboxamide

N-{2-[N-(5-bromo(3- isoquinolyl))carbamoyloxy]ethyl} {[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

methyl 3-{[2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy] carbonylamino} isoquinoline-5-carboxylate

{[(2-chloro-3-fluorophenyl) methyl]amino}-N- methyl-N-[2-(N- pyridino[3,4-d]pyridin-3- ylcarbamoyloxy)ethyl]carboxamide

(3S)-3-({[(2-chloro-3-fluorophenyl) methyl]amino}- N-methylcarbonylamino)-4- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] butanoic acid

N-{(2R)-2-[(tert-butoxy) carbonylamino]-3- hydroxypropyl}(3S)-3-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butanamide

N-((2R)-2-amino-3- hydroxypropyl)(3S)-3-({[(2- chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butanamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4- morpholin-4-yl-4- oxobutoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide

[((3S,2R)-1-{N-[(2-chloro-3- fluorophenyl)methyl]carbamoyl}-3- hydroxypyrrolidin-2-yl) methoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide

N-[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3- [N-(6-fluoro(3- isoquinolyl)) carbamoyloxy]propyl]-2- aminoacetamide

(2S)-N-[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]propyl]-2-amino-3- hydroxypropanamide

(2R)-N-[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]propyl]-2- amino-3- hydroxypropanamide

[(2S)-3-[(tert-butoxy)carbonylamino]- 2-({[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarbonylamino)propoxy]-N- (6-fluoro(3-isoquinolyl))carboxamide

[(2S)-3-amino-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N- (6-fluoro(3-isoquinolyl))carboxamide

(5S)-5-({[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarbonylamino)- 6-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl 2- (dimethylamino)acetate

N-((1S)-5-diazo-3-fluoro-1- {[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}- 5-azapent-5- enyl){[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

{[(2-chloro-3-fluorophenyl) methyl]amino}-N- methyl-N-[2-(N-pyridino[2,3- d]pyridin-7- ylcarbamoyloxy)ethyl] carboxamide

{[(2-chloro-3-fluorophenyl) methyl]amino}-N-(2- {N-[5-(hydroxymethyl)(3- isoquinolyl)]carbamoyloxy} ethyl)-N-methylcarboxamide

N-{2-[N-(8-bromo(3- isoquinolyl))carbamoyloxylethyl} {[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

N-{2-[N-(5-acetyl(3- isoquinolyl))carbamoyloxy]ethyl} {[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

3-{[2-({[(2-chloro-3- fluorophenyl)methyl] amino}-N- methylcarbonylamino)ethoxy] carbonylamino} isoquinoline-5-carboxamide

N-((1S)-4-amino-3-fluoro-1- {[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}butyl){[(2- chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide

(5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-6- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] hexyl dimethyl phosphate

N-{(1S)-4-(1,3- dioxobenzo[c]azolin-2-yl)-1-[(N-(3- isoquinolyl)carbamoyloxy) methyl]butyl}{[(2- chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide

N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl]-2- aminoacetamide

(2S)-N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl]-2- amino-3-hydroxypropanamide

(2R)-N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl]- 2-amino-3-hydroxypropanamide

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)- 5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl 2-(dimethylamino)acetate

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] pentyl dihydrogen phosphate

[(2S)-4-amino-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)butoxy]-N- (6-fluoro(3-isoquinolyl))carboxamide

N-[(3S)-3-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butyl]-2- aminoacetamide

(5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-6- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] hexyl (2S)-2-[(tert- butoxy)carbonylamino]-3- methylbutanoate

(5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-6- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl (2R)-2-[(tert-butoxy) carbonylamino]-3-methylbutanoate

(5S)-5-({[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarbonylamino)- 6-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] hexyl (2S)-2-amino-3- methylbutanoate

(5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-6- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl (2R)-2-amino-3- methylbutanoate

(5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-6-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl dihydrogen phosphate

N-((1S)-4-(amidinoamino)-1- {[N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]methyl}butyl){[(2- chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl] aminoamide

N-(4-{[(1E)-2-cyano-1-(methylamino)-2- azavinyl]amino}(1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl) {[(2-chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl (2S)-2-amino-3- hydroxypropanoate

(4S)-4-({[(2-chloro-3-fluorophenyl) methyl]amino}- N-methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] pentyl (2R)-2-amino-3- hydroxypropanoate

(4S)-4-({[(2-chloro-3-fluorophenyl) methyl]amino}- N-methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] pentyl (2S)-2-amino-3- methylbutanoate

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] pentyl (2R)-2-amino-3- methylbutanoate

{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methyl-N-[2-(N-pyridino[3,2-d]pyridin-6- ylcarbamoyloxy)ethyl]carboxamide

N-{(1S)-4-amino-1-[(N- pyridino[4,3-d]pyridin-3- ylcarbamoyloxy)methyl] butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

N-{(1S)-4-amino-1-[(N- pyridino[3,2-d]pyridin-6- ylcarbamoyloxy)methyl] butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

tert-butyl 4-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanoyl] piperazinecarboxylate

(4S)-N-{2-[(tert-butoxy) carbonylamino]ethyl}-4- ({[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarbonylamino)-5- [N-(6-fluoro(3-isoquinolyl))carbamoyloxy] pentanamide

N-{(2R)-2-[(tert-butoxy)carbonylamino]-3- hydroxypropyl}(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanamide

tert-butyl 3-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanoylamino] pyrrolidinecarboxylate

{[(2-chloro-3-fluorophenyl) methyl]amino}-N-{2- [N-(8-cyano(3-isoquinolyl)) carbamoyloxy]ethyl}- N-methylcarboxamide

(4S)-N-(2-aminoethyl)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-4- oxo-4-piperazinylbutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((2R)-2-amino-3- hydroxypropyl)(4S)-4-({[(2- chloro-3-fluorophenyl) methyl]amino}-N- methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] pentanamide

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]- N-pyrrolidin-3- ylpentanamide

(2S)-N-[(3S)-3-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butyl]- 2-amino-3-hydroxypropanamide

(2R)-N-[(3S)-3-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butyl]-2- amino-3-hydroxypropanamide

N-(4-[((1E)-1-amino-2-cyano-2- azavinyl)amino](1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}butyl){[(2- chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide

N-(4-[((1E)-1-amino-2-carbamoyl-2- azavinyl)amino](1S)-1- {[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}butyl){[(2- chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

N-((1S)-4-{[(1Z)-1- (dimethylamino)-2-cyano-2- azavinyl]amino}-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}butyl){[(2- chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

N-(6-bromo(3-isoquinolyl)) [2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino) ethoxy]carboxamide

N-((1S)-4-(1,3- dioxobenzo[c]azolin-2-yl)-1- {[N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]methyl}butyl){[(2- chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

(2S)-N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5- (N-pyridino[4,3- d]pyridin-3-ylcarbamoyloxy) pentyl]-2-[(tert- butoxy)carbonylamino]-3- hydroxypropanamide

(2S)-N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N- pyridino[4,3- d]pyridin-3-ylcarbamoyloxy) pentyl]-2-amino-3- hydroxypropanamide

(2S)-N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N- pyridino[3,2- d]pyridin-6-ylcarbamoyloxy) pentyl]-2-[(tert- butoxy)carbonylamino]-3- hydroxypropanamide

(2S)-N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5- (N-pyridino[3,2- d]pyridin-6-ylcarbamoyloxy) pentyl]-2-amino-3- hydroxypropanamide

(3S)-3-({[(2-chloro-3-fluorophenyl) methyl]amino}- N-methylcarbonylamino)-4- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-1- [(methoxyphosphinyl)methyl] butyl dimethyl phosphate

methyl 3-{[2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy] carbonylamino} isoquinoline-6-carboxylate

N-((1S)-3-carbamoyl-1- {[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}propyl){[(2- chloro-3-fluorophenyl)methyl] amino}-N- methylcarboxamide

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] pentanoic acid

methyl (4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy) pentanoate

N-[(1S)-4-amino-1-({N- [5-(trifluoromethyl)(2- pyridyl)]carbamoyloxy}methyl) butyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-3-amidino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}propyl){[(2- chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide

N-((1S)-4-(ethylamino)-1- {[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}-4-iminobutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy) pentanoic acid

N-(7-bromo(3- isoquinolyl))[2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy] carboxamide

(5S)-5-({[(2,3-difluorophenyl) methyl]amino}-N- methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy)hexyl 2- (dimethylamino)acetate

(5S)-5-({[(2,3-difluorophenyl) methyl]amino}-N- methylcarbonylamino)-6- (N-(3-isoquinolyl)carbamoyloxy) hexyl dihydrogen phosphate

(5S)-5-({[(2,3-difluorophenyl) methyl]amino}-N- methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy) hexyl (2S)-2-amino-3- methylbutanoate

(5S)-5-({[(2,3-difluorophenyl) methyl]amino}-N- methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy) hexyl (2R)-2-amino-3- methylbutanoate

(5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-6- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl (2S)-3-(tert- butoxy)-2-[(tert-butoxy) carbonylamino]propanoate

(5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-6- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] hexyl (2S)-2-amino-3- hydroxypropanoate

(5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-6- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] hexyl (2R)-3-(tert- butoxy)-2-[(tert-butoxy) carbonylamino]propanoate

(5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-6- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] hexyl (2R)-2-amino-3- hydroxypropanoate

methyl (5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N- pyridino[4,3- d]pyridin-3-ylcarbamoyloxy) hexanoate

(5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-6- (N-pyridino[4,3- d]pyridin-3-ylcarbamoyloxy) hexanoic acid

N-{(1S)-5-hydroxy-1-[(N- pyridino[4,3-d]pyridin-3- ylcarbamoyloxy)methyl]pentyl} {[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

methyl (5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N- pyridino[3,4-d]pyridin-3- ylcarbamoyloxy)hexanoate

(5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-6- (N-pyridino[3,4- d]pyridin-3-ylcarbamoyloxy) hexanoic acid

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}- 3,4-dihydroxybutyl){[(3-fluorophenyl) methyl]amino}- N-methylcarboxamide

methyl 3-{[2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy] carbonylamino} isoquinoline-7-carboxylate

N-((1S)-5-diazo-3,3-difluoro-1- {[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}- 5-azapent-5- enyl){[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

[(2S)-5-amino-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)pentyloxy]- N-(5-chloro(2- pyridyl))carboxamide

[(2S)-3-amino-2-({[(3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]- N-(6-fluoro(3- isoquinolyl))carboxamide

N-{(1S)-1-[(N-pyridino[3,4- d]pyridin-3- ylcarbamoyloxy)methyl]but-3- enyl}{[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

N-{(1S)-3,4-dihydroxy-1- [(N-pyridino[3,4- d]pyridin-3-ylcarbamoyloxy) methyl]butyl}{[(2- chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

N-((1S)-4-amino-3,3-difluoro-1- {[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}butyl){[(2- chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

(4S)-4-({[(2-chloro-3-fluorophenyl) methyl]amino}- N-methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]- 2-hydroxypentyl (2S)-2- amino-3-methylbutanoate

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-2- hydroxypentyl (2R)- 2-amino-3-methylbutanoate

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-2- hydroxypentyl (2S)-2- amino-3-hydroxypropanoate

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-2- hydroxypentyl (2R)- 2-amino-3-hydroxypropanoate

N-[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]propyl][4- (phenylcarbonyl)phenyl]carboxamide

N-[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]propyl][3- (phenylcarbonyl)phenyl]carboxamide

N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl][4- (phenylcarbonyl)phenyl]carboxamide

N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl][3- (phenylcarbonyl)phenyl]carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl] amino}-N-methylcarbonylamino)-3- [(phenylmethoxy) carbonylamino]propoxy]-N-(6- fluoro(3-isoquinolyl))carboxamide

N-[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] propyl]-2-[(tert- butoxy)carbonylamino]acetamide

{[(2-chloro-3-fluorophenyl)methyl]amino}-N- (2-{N-[7-(hydroxymethyl)(3- isoquinolyl)]carbamoyloxy}ethyl)-N- methylcarboxamide

{[(2-chloro-3-fluorophenyl)methyl]amino}- N-(2-{N-[6-(hydroxymethyl)(3- isoquinolyl)]carbamoyloxy}ethyl)-N- methylcarboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)pent-4-enyloxy]- N-(3-isoquinolyl)carboxamide

{[(5-bromo-2- chlorophenyl)methyl]amino}-N-(2- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}- N-methylcarboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)pent- 4-enyloxy]-N-(5- chloro(2-pyridyl))carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-4,5- dihydroxypentyloxy]- N-(3-isoquinolyl)carboxamide

methyl 4-chloro-3-{[(N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-N- methylcarbamoyl)amino]methyl}benzoate

[(2S,4R)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5- dihydroxypentyloxy]-N- (3-isoquinolyl)carboxamide

[(2S,4S)-2-(([(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5- dihydroxypentyloxy]-N- (3-isoquinolyl)carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-4,5- dihydroxypentyloxy]- N-(5-chloro(2-pyridyl))carboxamide

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-2- hydroxy-5-(N-(3- isoquinolyl)carbamoyloxy) pentyl dihydrogen phosphate

[(2S)-2-({[(3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5- dihydroxypentyloxy]-N- (3-isoquinolyl)carboxamide

(5S)-5-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy)hexyl dihydrogen phosphate

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-2- hydroxy-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl 2- (dimethylamino)acetate

N-{(1S)-4-(1,3- dioxobenzo[c]azolin-2-yl)-1-[(N- pyridino[3,4-d]pyridin-3- ylcarbamoyloxy)methyl]butyl} {[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

N-{(1S)-4-amino-l-[(N- pyridino[3,4-d]pyridin-3- ylcarbamoyloxy)methyl]butyl} {[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- hydroxypentyloxy]-N- (3-isoquinolyl)carboxamide

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy) pentyl dihydrogen phosphate

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-oxo-5- piperazinylpentyloxy]-N-(3- isoquinolyl)carboxamide

tert-butyl 4-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoyl] piperazinecarboxylate

N-{(1S)-1-[(N-(3-isoquinolyl) carbamoyloxy)methyl]but-3-enyl}{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-3,4-dihydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy) methyl]butyl}{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S,3S)-3,4-dihydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy) methyl]butyl}{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S,3R)-3,4-dihydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy) methyl]butyl}{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

({[2-chloro-5-(hydroxymethyl) phenyl]methyl}amino)-N-{2-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]ethyl}-N- methylcarboxamide

(4S)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-2- hydroxy-5-(N-(3- isoquinolyl)carbamoyloxy) pentyl dihydrogen phosphate

N-[(2S)-2-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3- isoquinolyl)carbamoyloxy)propyl]-2- aminoacetamide

N-{(1S)-4-amino-3,3-difluoro-1-[(N-(3- isoquinolyl)carbamoyloxy) methyl]butyl}{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-4-amino-3,3-difluoro-1-[(N-(3- isoquinolyl)carbamoyloxy) methyl]butyl}{[(2- chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide

(4S,2R)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]- 2-hydroxypentyl dihydrogen phosphate

(2S,4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-2- hydroxypentyl dihydrogen phosphate

(5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy) hexyl diethyl phosphate

N-{(1S)-1-[(N-pyridino[4,3- d]pyridin-3- ylcarbamoyloxy)methyl]but-3- enyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-3,4-dihydroxy-1- [(N-pyridino[4,3- d]pyridin-3-ylcarbamoyloxy) methyl]butyl}{[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

N-[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3- isoquinolyl)carbamoyloxy)propyl]- 2-aminoacetamide

(5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy) hexyl dimethyl phosphate

(5S)-5-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy)hexyl dihydrogen phosphate

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] hexanoate

(4S,2R)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-2- hydroxy-5-(N-(3- isoquinolyl)carbamoyloxy) pentyl dihydrogen phosphate

(2S,4S)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)- 2-hydroxy-5-(N-(3- isoquinolyl)carbamoyloxy) pentyl dihydrogen phosphate

[(2S)-2-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6- hydroxyhexyloxy]-N-(6- fluoro(3-isoquinolyl))carboxamide

(5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] hexyl dimethyl phosphate

(5S)-5-({[(2,3-difluorophenyl) methyl]amino}-N- methylcarbonylamino)-6- (N-(6-fluoro(3- isoquinolyl))carbamoyloxy] hexyl dihydrogen phosphate

[(2S)-2-({[(2,3-difluorophenyl) methyl]amino}-N-methyl- carbonylamino)-4-oxo-4- piperazinylbutoxy]- N-(3-isoquinolyl)carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino)- N-methylcarbonylamino)-4- oxo-4-piperazinylbutoxy]-N- (3-isoquinolyl)carboxamide

[(2S,4S)-2-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5- dihydroxypentyloxy]-N- (6-fluoro(3-isoquinolyl))carboxamide

[(2S,4R)-2-({[(2,3- difluorophenyl)methyl]amino}- N-methylcarbonylamino)-4,5- dihydroxypentyloxy]- N-(6-fluoro(3-isoquinolyl))carboxamide

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(5- phenylisoxazol-3- yl)carbamoyloxy]hexanoate

methyl (5R)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy)hexanoate

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6- [N-(5-chloro(2- pyridyl))carbamoyloxy]hexanoate

N-{(1S)-3,4-dihydroxy-1-[(N- quinazolin-2-ylcarbamoyloxy) methyl]butyl}{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

[(2S,4R)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5- dihydroxypentyloxy]- N-benzothiazol-2-ylcarboxamide

methyl (4S)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoate

methyl (4S)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanoate

N-{(1S)-4-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy) methyl]butyl}{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}-4-hydroxybutyl) {[(2,3-difluorophenyl)methyl] amino}-N-methylcarboxamide

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6- [N-(5-phenyl(1,3,4- thiadiazol-2-yl)) carbamoyloxy]hexanoate

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4- fluorophenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4- chlorophenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4- methylphenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4- methoxyphenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(2- chlorophenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate

[(2R)-2-({[(2,3-difluorophenyl) methyl]amino}-N- methylcarbonylamino)-6- hydroxyhexyloxy]-N-(3- isoquinolyl)carboxamide

(5R)-5-({[(2,3-difluorophenyl) methyl]amino}-N- methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy) hexyl dimethyl phosphate

(5R)-5-({[(2,3-difluorophenyl) methyl]amino}-N- methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy) hexyl dihydrogen phosphate

(5S)-5-({[(2,3-difluorophenyl) methyl]amino}-N- methylcarbonylamino)-6- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] hexyl hydroxysulfonate

[(2R,4R)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5- dihydroxypentyloxy]-N- (6-fluoro(3-isoquinolyl))carboxamide

[(2R)-3-((4R)-2-oxo(1,3- dioxolan-4-yl))-2-({[(2- chloro-3-fluorophenyl) methyl]amino}-N- methylcarbonylamino)propoxy]- N-(6-fluoro(3-isoquinolyl))carboxamide

[(2S)-2-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-4- oxo-4-piperazinylbutoxy]- N-(6-fluoro(3-isoquinolyl))carboxamide

(4S)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy] pentyl dihydrogen phosphate

(4S)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy) pentanoic acid

(4S)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N- (6-fluoro(3-isoquinolyl))carbamoyloxy] pentanoic acid

tert-butyl 4-[(4S)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoyl] piperazinecarboxylate

tert-butyl 4-[(4S)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanoyl] piperazinecarboxylate

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N- [5-(trifluoromethyl)(2- pyridyl)]carbamoyloxy}hexanoate

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4- bromophenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4- cyanophenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(2- fluorophenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate

(4S)-4-({[(2,3-difluorophenyl) methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy) pentyl dihydrogen phosphate

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]- 2-hydroxypentyl hydroxysulfonate

N-((1S)-5-hydroxy-1- {[N-(5-phenylisoxazol-3- yl)carbamoyloxy]methyl}pentyl){[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

(2S,4R)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-2- hydroxypentyl dihydrogen phosphate

(2R,4R)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy}-2- hydroxypentyl dihydrogen phosphate

N-((3S,1R)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-3,4- dihydroxybutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1R)-1-[((4S)-2-oxo(1,3- dioxolan-4-yl))methyl]- 2-[N-(6-fluoro(3-isoquinolyl)) carbamoyloxylethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

N-{(1S)-1-[(N-(3-isoquinolyl) carbamoyloxy)methyl]-4-oxo-4- piperazinylbutyl}{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}- 4-oxo-4-piperazinylbutyl){[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5- (tert-butyl)isoxazol- 3-yl]carbamoyloxy}hexanoate

(4S,2R)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5- [N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]-2-hydroxypentyl dihydrogen phosphate

({(1S,3R)-1-[(N-benzoxazol-2- ylcarbamoyloxy)methyl]-3,4- dihydroxybutyl}methylamino)-N- [(2-chloro-3- fluorophenyl)methyl]carboxamide

[((1S,3R)-1-{[N-(5-chlorobenzoxazol- 2-yl)carbamoyloxy]methyl}-3,4- dihydroxybutyl)methylamino]-N- [(2-chloro-3- fluorophenyl)methyl]carboxamide

methyl (5S)-5-({N-[(2,3- difluorophenyl)methyl]carbamoyl} methylamino)-6- {N-[5-(4-methylphenyl)isoxazol-3- yl]carbamoyloxy}hexanoate

N-{1-[((4R)-2,2-dimethyl(1,3-dioxolan-4- yl))methyl](1S)-2-[N-(5-phenylisoxazol-3- yl)carbamoyloxy]ethy}{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S,3R)-3,4-dihydroxy-1- {[N-(5-phenylisoxazol- 3-yl)carbamoyloxy]methyl} butyl){[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5- (trifluoromethyl)isoxazol-3- yl]carbamoyloxy}hexanoate

(2S,4R)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6- fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl diethyl phosphate

(2R,4R)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-2- hydroxypentyl diethyl phosphate

(3S,1R)-3-({[(2,3- difluorophenyl)methyl]amino}- N-methylcarbonylamino)-1- [(ethoxyphosphinyl)methyl]-4-(N-(3- isoquinolyl)carbamoyloxy) butyl diethyl phosphate

(4S,2R)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-2- hydroxy-5-(N-(3- isoquinolyl)carbamoyloxy) pentyl diethyl phosphate

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}-4-hydroxy-3- (hydroxymethyl)butyl){[(2-chloro- 3-fluorophenyl)methyl]amino}- N-methylcarboxamide

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4- fluorophenyl)isoxazol-3-yl] carbamoyloxy}hexanoate

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4- bromophenyl)isoxazol-3- yl]carbamoyloxy}hexanoate

N-[(1S)-1-({N-[5-(4- fluorophenyl)isoxazol-3- yl]carbamoyloxy}methyl)-5- hydroxypentyl]{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(1S)-1-({N-[3-(4- bromophenyl)isoxazol-5- yl]carbamoyloxy}methyl)-5- hydroxypentyl]{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(1S)-1-({N-[3-(4- cyanophenyl)isoxazol-5- yl]carbamoyloxy}methyl)-5- hydroxypentyl]{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(3- phenylisoxazol-5- yl)carbamoyloxy]hexanoate

N-((1S)-5-hydroxy-1- {[N-(3-phenylisoxazol-5- yl)carbamoyloxy]methyl}pentyl){[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

[(2S)-5-({[(tert- butoxy)carbonylamino] sulfonyl}amino)-2-({[(2- chloro-3-fluorophenyl) methyl]amino}-N- methylcarbonylamino) pentyloxy]-N-(6-fluoro(3- isoquinolyl))carboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-4- (sulfamoylamino)butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]-2- hydroxyacetamide

N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]-2,3- dihydroxypropanamide

N-((1S)-4-{[(dimethylamino) sulfonyl]amino}-1- {[N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]methyl}butyl){[(2- chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}- 4-[(propylsulfonyl)amino]butyl) {[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-3,3-difluoro-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-4- hydroxybutyl)([(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

(5S)-5-({[(2,3-difluorophenyl) methyl]amino}-N- methylcarbonylamino)-6- [N-(5-phenylisoxazol-3- yl)carbamoyloxy] hexyl dihydrogen phosphate

[(2S,4R)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5- dihydroxypentyloxy]-N- (5,6-dimethylbenzothiazol-2- yl)carboxamide

N-[4-({(1E)-2-cyano-1-[(2- hydroxyethyl)amino]- 2-azavinyl}amino)(1S)-1- {[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}butyl]{[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

(4S,2R)-5-(N-benzothiazol-2- ylcarbamoyloxy)-4- ({[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarbonylamino)-2- hydroxypentyl dihydrogen phosphate

N-[4-({(1E)-2-cyano-1- [(2-hydroxyethyl)amino]-2- azavinyl}amino)(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy) methyl]butyl]{[(2-chloro- 3-fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[4-({(1E)-2-cyano-1-[(3- hydroxypropyl)amino]-2- azavinyl}amino)(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl] {[(2-chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide

[(2S,4R)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5- dihydroxypentyloxy]-N- (6-methylbenzothiazol-2-yl)carboxamide

N-{4-[((1E)-2-cyano-1-{[2-hydroxy-1- (hydroxymethyl)ethyl]amino}-2- azavinyl)amino](1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl} {[(2-chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-2,2- difluoro-5-[N-(6- fluoro(3-isoquinolyl))carbamoyloxy] pentyl dimethyl phosphate

{N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl] carbamoyl}methyl dimethyl phosphate

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-2,2- difluoro-5-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]pentyl dihydrogen phosphate

(4S,2R)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-[N- (5-phenylisoxazol-3-yl)carbamoyloxy] pentyl diethyl phosphate

(4S,2R)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-[N-(5- phenylisoxazol-3-yl)carbamoyloxy]pentyl dihydrogen phosphate

[(2S,4R)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5- dihydroxypentyloxy]-N- (6-chlorobenzothiazol-2-yl)carboxamide

[(2S,4R)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5- dihydroxypentyloxy]-N- (6-fluorobenzothiazol-2-yl)carboxamide

[(2S,4R)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5- dihydroxypentyloxy]-N- (5,6-difluorobenzothiazol-2-yl)carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-hydroxy-4,4- dimethylpentyloxy]-N-(6-fluoro(3- isoquinolyl))carboxamide

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- [N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-2,2- dimethylpentyl dihydrogen phosphate

N-[(1S)-1-({N-[5-(4- chlorophenyl)isoxazol-3- yl]carbamoyloxy}methyl)-5- hydroxypentyl]{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(1S)-1-({N-[5-(2- chlorophenyl)isoxazol-3- yl]carbamoyloxy}methyl)-5- hydroxypentyl]{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(1S)-1-({N-[5-(3- fluorophenyl)isoxazol-3- yl]carbamoyloxy}methyl)-5- hydroxypentyl]{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-{1-[((4R)-2,2-dimethyl(1,3- dioxolan-4-yl))methyl](1S)-2-[N- (3-phenylisoxazol-5- yl)carbamoyloxy]ethyl} {[(2-chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide

N-((1S,3R)-3,4-dihydroxy-1- {[N-(3-phenylisoxazol- 5-yl)carbamoyloxy]methyl} butyl){[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(1-methyl- 5-phenylpyrazol-3-yl) carbamoyloxy]hexanoate

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N- (1-methyl-3-phenylpyrazol-5- yl)carbamoyloxy]hexanoate

N-((1S)-5-hydroxy-1-{[N-(1-methyl-5- phenylpyrazol-3-yl) carbamoyloxy]methyl}pentyl){[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-5-hydroxy-1-{[N-(1-methyl-3- phenylpyrazol-5- yl)carbamoyloxy]methyl}pentyl){[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-{1-[((4R)-2,2-dimethyl(1,3-dioxolan- 4-yl))methyl](1S)-2-[N-(5- phenyl(1,2,4-oxadiazol-3- yl))carbamoyloxy]ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

N-((1S,3R)-3,4-dihydroxy-1- {[N-(5-phenyl(1,2,4- oxadiazol-3-yl))carbamoyloxy] methyl}butyl){[(2- chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide

ethyl 2-({N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl] carbamoyl}amino)acetate

N-[(1S)-1-({N-[5-(3- chlorophenyl)isoxazol-3- yl]carbamoyloxy}methyl)-5- hydroxypentyl]{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

methyl (5S)-5-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(4-methyl- 3-phenylisoxazol-5-yl) carbamoyloxy]hexanoate

2-[((1E)-1-{[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy) pentyl]amino}-2-carbamoyl-2-azavinyl) amino]ethyl dihydrogen phosphate

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-{[(2- hydroxyethyl)amino]carbonylamino} pentyloxy]-N-(6-fluoro(3- isoquinolyl))carboxamide

N-{1-[((4R)-2,2-dimethyl(1,3-dioxolan-4- yl))methyl](1S)-2-[N-(5-phenylisoxazol-3- yl)carbamoyloxy]ethyl}{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S,3R)-3,4-dihydroxy-1- {[N-(5-phenylisoxazol- 3-yl)carbamoyloxy]methyl}butyl){[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

(4S,2R)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-[N- (5-phenylisoxazol-3-yl)carbamoyloxy] pentyl diethyl phosphate

(3S,1R)-3-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-1- [(ethoxyphosphinyl)methyl]-4- [N-(5-phenylisoxazol- 3-yl)carbamoyloxy]butyl diethyl phosphate

(4S,2R)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-(N-(3- isoquinolyl)carbamoyloxy) pentyl dihydrogen phosphate

(4S,2R)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-[N-(5- phenylisoxazol-3-yl)carbamoyloxy]pentyl dihydrogen phosphate

2-({N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]carbamoyl} amino)ethyl dihydrogen phosphate

N-[(1S,3R)-1-({N-[5-(3- fluorophenyl)isoxazol-3- yl]carbamoyloxy}methyl)-3,4- dihydroxybutyl]{[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

N-(1-[((4R)-2,2-dimethyl(1,3-dioxolan-4- yl))methyl](1S)-2-{N-[5-(3- fluorophenyl)isoxazol-3- yl]carbamoyloxy}ethyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-1-[(2- hydroxyethoxy)methyl]ethyl} {[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

2-[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]propoxy]ethyl dihydrogen phosphate

N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl][(3- hydroxypropyl)amino]carboxamide

(4S,2R)-5-[N-(6-chlorobenzothiazol-2- yl)carbamoyloxy]-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxypentyl dihydrogen phosphate

N-[4-({(1E)-2-carbamoyl-1-[(2- hydroxyethyl)amino]-2- azavinyl}amino)(1S)-1-[(N- (3-isoquinolyl)carbamoyloxy) methyl]butyl]{[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

N-[4-({(1E)-2-carbamoyl-1-[(2- hydroxyethyl)amino]-2- azavinyl}amino)(1S)-1-{[N- (6-fluoro(3-isoquinolyl))carbamoyloxy] methyl}butyl]{[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

N-[4-({(1E)-2-cyano-1-[(3-hydroxy-2,2- dimethylpropyl)amino]-2- azavinyl}amino)(1S)-1- {[N-(6-fluoro(3-isoquinolyl)) carbamoyloxy]methyl}butyl]{[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

2-[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]propoxy]ethyl dimethyl phosphate

(4S,2R)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-{N-[5-(3- fluorophenyl)isoxazol-3-yl]carbamoyloxy}- 2-hydroxypentyl diethyl phosphate

(4S,2R)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-{N-[5-(3- fluorophenyl)isoxazol-3-yl]carbamoyloxy}- 2-hydroxypentyl dihydrogen phosphate

(4S,2R)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6- fluorobenzothiazol-2-yl)carbamoyloxy]- 2-hydroxypentyl dihydrogen phosphate

3-({N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl] carbamoyl}amino)-2,2- dimethylpropyl dimethyl phosphate

3-({N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] pentyl]carbamoyl} amino)-2,2-dimethylpropyl dihydrogen phosphate

(4S,2R)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-[N-(3- phenylisoxazol-5-yl)carbamoyloxy]pentyl dihydrogen phosphate

N-{(1S)-2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-1- [(3-hydroxy-2,2- dimethylpropoxy)methyl]ethyl} {[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[4-({(1E)-2-cyano-1-[(3-hydroxy-2,2- dimethylpropyl)amino]-2- azavinyl}amino)(1S)-1- [(N-benzothiazol-2- ylcarbamoyloxy)methyl]butyl] {[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[4-({(1E)-2-cyano-1- [(2-hydroxyethyl)amino]-2- azavinyl}amino)(1S)-1- [(N-benzothiazol-2- ylcarbamoyloxy)methyl]butyl] {[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{1-[((4R)-2,2-dimethyl(1,3-dioxolan-4- yl))methyl](1S)-2-(N-(3- isoquinolyl)carbamoyloxy)ethyl}{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-(1-[((4R)-2,2-dimethyl(1,3-dioxolan-4- yl))methyl](1S)-2-{N-[5-(3- chlorophenyl)isoxazol- 3-yl]carbamoyloxy}ethyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(1S,3R)-1-({N-[5-(3- chlorophenyl)isoxazol-3- yl]carbamoyloxy}methyl)-3,4- dihydroxybutyl]{[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

3-[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]propoxy]-2,2- dimethylpropyl dihydrogen phosphate

(4S,2R)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-{N-[5-(3- chlorophenyl)isoxazol-3-yl] carbamoyloxy}-2- hydroxypentyl dihydrogen phosphate

N-{(1S)-4-amino-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl} {[(2,3-difluorophenyl)methyl]amino}- N-methylcarboxamide

N-((1S)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl) {[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide

N-{1-[({(1E)-2-cyano-1- [(3-hydroxypropyl)amino]- 2-azavinyl}amino)methyl](1S)- 2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl} {[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-1-[(N-benzothiazol-2- ylcarbamoyloxy)methyl]-5-diazo-5-azapent- 5-enyl}{[(2,3-difluorophenyl)methyl] amino}-N-methylcarboxamide

N-{(1S)-4-amino-1-[(N-benzothiazol-2- ylcarbamoyloxy)methyl]butyl}{[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-5-diazo-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}-5-azapent-5- enyl){[(2,3-difluorophenyl)methyl] amino}-N-methylcarboxamide

2-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoyl- amino]ethyl dihydrogen phosphate

3-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy) pentanoylamino]-2,2- dimethylpropyl dihydrogen phosphate

3-{[(5S)-5-({[(2,3- difluorophenyl)methyl] amino}-N-methylcarbonylamino)- 6-(N-(3-isoquinolyl)carbamoyloxy) hexyl]oxycarbonyl}propanoic acid

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-N- (2-hydroxyethyl)-5-(N- (3-isoquinolyl)carbamoyloxy)pentanamide

N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] pentyl][(3-hydroxy-2,2- dimethylpropyl)amino]carboxamide

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-N- (3-hydroxypropyl)-5- (N-(3-isoquinolyl)carbamoyloxy) pentanamide

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-N- (3-hydroxy-2,2- dimethylpropyl)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanamide

(4S)-N-((2S)-2-hydroxypropyl)-4- ({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanamide

N-((2R)-2-hydroxypropyl)(4S)- 4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy) pentanamide

N-{(1S)-1-[((2S)-2,3- dihydroxypropoxy)methyl]-2- [N-(6-fluoro(3-isoquinolyl))carbamoyloxy] ethyl}{[(2-chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide

2-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy) pentanoylamino] ethyl ditert-butyl phosphate

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-[4-(2- hydroxyethyl)piperazinyl]-5- oxopentyloxy]-N-(3- isoquinolyl)carboxamide

N-((1S)-3-carbamoyl-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}propyl){[(2,3- difluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-4-amino-1-{[N-(3- phenylisoxazol-5- yl)carbamoyloxy]methyl}butyl){[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

methyl (4S)-5-(N- benzothiazol-2-ylcarbamoyloxy)- 4-({[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarbonylamino)pentanoate

tert-butyl 4-[(4S)-5-(N-benzothiazol-2- ylcarbamoyloxy)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)pentanoyl] piperazinecarboxylate

tert-butyl 4-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3- phenylisoxazol-5- yl)carbamoyloxy]pentanoyl] piperazinecarboxylate

N-((1S)-4-oxo-1-{[N-(3-phenylisoxazol- 5-yl)carbamoyloxy]methyl}-4- piperazinylbutyl){[(2- chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-1-[(N-benzothiazol-2- ylcarbamoyloxy)methyl]-4-oxo-4- piperazinylbutyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

tert-butyl 4-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(5- phenylisoxazol-3- yl)carbamoyloxy]pentanoyl] piperazinecarboxylate

N-((1S)-4-oxo-1-{[N- (5-phenylisoxazol-3- yl)carbamoyloxy]methyl}-4- piperazinylbutyl){[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

2-{4-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy) pentanoyl]piperazinyl} ethyl dihydrogen phosphate

2-{4-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoyl] piperazinyl}ethyl dimethyl phosphate

ethyl 2-({N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3- phenylisoxazol- 5-yl)carbamoyloxy]pentyl]carbamoyl} amino)acetate

(4S)-5-(N-benzothiazol-2- ylcarbamoyloxy)-4-({[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarbonylamino)pentanoic acid

N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3- phenylisoxazol- 5-yl)carbamoyloxy]pentyl][(2- hydroxyethyl)amino]carboxamide

N-{(1S)-1-[((2S)-2,3- dihydroxypropoxy)methyl]-2- (N-(3-isoquinolyl)carbamoyloxy)ethyl} {[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

methyl (4S)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(5- phenylisoxazol- 3-yl)carbamoyloxy]pentanoate

methyl (4S)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3- phenylisoxazol- 5-yl)carbamoyloxy]pentanoate

2-({N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3- phenylisoxazol-5- yl)carbamoyloxy]pentyl] carbamoyl}amino)ethyl dimethyl phosphate

2-({N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N- (3-phenylisoxazol-5- yl)carbamoyloxy]pentyl] carbamoyl}amino)ethyl dihydrogen phosphate

ethyl 2-({N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl] carbamoyl}amino) acetate

tert-butyl 4-[(4S)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(5- phenylisoxazol-3- yl)carbamoyloxy]pentanoyl] piperazinecarboxylate

[(2S)-2-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-oxo-5- piperazinylpentyloxy]-N-(5- phenylisoxazol-3-yl)carboxamide

tert-butyl 4-[(4S)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3- phenylisoxazol-5- yl)carbamoyloxy]pentanoyl] piperazinecarboxylate

[(2S)-2-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-oxo-5- piperazinylpentyloxy]-N-(3- phenylisoxazol-5-yl)carboxamide

N-{(1S)-1-[(2- hydroxyethoxy)methyl]-2-(N-(3- isoquinolyl)carbamoyloxy)ethyl} {[(2-chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

2-[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3- isoquinolyl)carbamoyloxy)propoxy] ethyl dihydrogen phosphate

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)-2,2- dimethylpentyl dihydrogen phosphate

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-hydroxy- 4,4-dimethylpentyloxy]-N- (3-isoquinolyl)carboxamide

(2R)-3-[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3- isoquinolyl)carbamoyloxy)propoxy]-2- hydroxypropyl dihydrogen phosphate

2-({N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy) pentyl]carbamoyl} amino)ethyl dimethyl phosphate

N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl][(2- hydroxyethyl)amino]carboxamide

2-({N-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy) pentyl]carbamoyl} amino)ethyl dihydrogen phosphate

methyl (4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3- phenylisoxazol-5- yl)carbamoyloxy]pentanoate

tert-butyl 4-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3- phenylisoxazol-5- yl)carbamoyloxy]pentanoyl]-1,4- diazaperhydroepinecarboxylate

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-(1,4- diazaperhydroepinyl)-5-oxopentyloxy]- N-(3-phenylisoxazol-5-yl)carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- (4-methylpiperazinyl)-5- oxopentyloxy]-N-(3-phenyl- isoxazol-5-yl)carboxamide

N-((1S)-4-hydroxy-3,3-dimethyl-1- {[N-(3-phenylisoxazol-5- yl)carbamoyloxy]methyl}butyl) {[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

methyl 4-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy) pentanoyl]piperazine-2-carboxylate

N-{(1S)-4-[3- (hydroxymethyl)piperazinyl]-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]- 4-oxobutyl}{[(2- chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

tert-butyl 4-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoyl]-2- (hydroxymethyl)piperazinecarboxylate

(4S,2R)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5- [N-(3-phenylisoxazol-5- yl)carbamoyloxy]pentyl diethyl phosphate

N-{(1S)-4-[(3S)-3- (hydroxymethyl)piperazinyl]-1- [(N-(3-isoquinolyl) carbamoyloxy)methyl]-4- oxobutyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

(4S)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy) pentyl ditert-butyl phosphate

N-((1S)-4-hydroxy-4-methyl-1- {[N-(3-phenylisoxazol-5- yl)carbamoyloxy]methyl} pentyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{1-[((2R)-2,3- dihydroxypropoxy)methyl](1S)-2- (N-(3-isoquinolyl)carbamoyloxy)ethyl} {[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{1-[((2R)-2,3- dihydroxypropoxy)methyl](1S)-2- (N-(3-isoquinolyl)carbamoyloxy)ethyl}- N-((2S)-2,3-dihydroxypropyl) {[(2-chloro-3-fluorophenyl)methyl] amino}carboxamide

N-{4-[(3R)-3- (hydroxymethyl)piperazinyl](1S)-1- [(N-(3-isoquinolyl)carbamoyloxy)methyl]- 4-oxobutyl}{[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

(2S)-3-[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3- isoquinolyl)carbamoyloxy)propoxy]-2- hydroxypropyl dihydrogen phosphate

(2S)-3-[(2S)-2-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3- isoquinolyl)carbamoyloxy)propoxy]-2- hydroxypropyl dihydrogen phosphate

N-{(1S)-1-[((2S)-2,3- dihydroxypropoxy)methyl]-2- (N-(3-isoquinolyl)carbamoyloxy)ethyl} {[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide

[(2R,4R)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5- dihydroxypentyloxy]- N-(3-isoquinolyl)carboxamide

[(4S,2R)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5- dihydroxypentyloxy]-N- (3-isoquinolyl)carboxamide

(2S,4R)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5- (N-(3-isoquinolyl)carbamoyloxy)pentyl dihydrogen phosphate

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- imidazo[2,1-c]piperazin- 7-yl-5-oxopentyloxy]-N-(3- isoquinolyl)carboxamide

[(2R)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-oxo-5- piperazinylpentyloxy]-N- (3-isoquinolyl)carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- oxo-5-(1,2,4- triazolo[3,4-c]piperazin-7- yl)pentyloxy]-N-(3- isoquinolyl)carboxamide

N-((1S)-4-[(tert-butoxy)carbonylamino]- 3,3-difluoro-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy] methyl}butyl){[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

N-((1S)-4-carbonylamino-3,3- difluoro-1-{[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]methyl}butyl) {[(2-chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

[(2S)-2-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-4- imidazol-2-ylbutoxy]-N-(6- fluoro(3-isoquinolyl))carboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}- 4-(piperazinylcarbonylamino) butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-4,4- difluoro-5-hydroxy-5- methylhexyloxy]-N-(6-fluoro(3- isoquinolyl))carboxamide

N-{(1S)-4-imidazo[5,1- c]piperazin-7-yl-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl] butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]- 4-(1,2,4-triazolo[3,4- c]piperazin-7-yl)butyl}{[(2-chloro- 3-fluorophenyl)methyl]amino}- N-methylcarboxamide

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-2,2- difluoro-5-[N-(6- fluoro(3-isoquinolyl)) carbamoyloxy]pentyl 4- nitrobenzoate

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-2,2- difluoro-5-{N-[5-(3- fluorophenyl)isoxazol-3-yl] carbamoyloxy}pentyl 4- nitrobenzoate

N-[(1S)-3,3-difluoro-1-({N-[5-(3- fluorophenyl)isoxazol-3-yl] carbamoyloxy}methyl)- 4-hydroxybutyl]{[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

N-((1S)-4-carbonylamino-1- {[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl} butyl){[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}- 4-[(2-hydroxy- 2-methylpropyl)amino]butyl){[(2-chloro- 3-fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-4-[bis(2-hydroxy-2- methylpropyl)amino]-1- {[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl) {[(2-chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-3-[(2,2,2- trifluoroethyl)amino]propoxy]-N-(3- isoquinolyl)carboxamide

[(2S)-3-[(2,2-difluoroethyl)amino]-2- ({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-(3- isoquinolyl)carboxamide

methyl 2-{[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3- isoquinolyl)carbamoyloxy) propyl]amino}acetate

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-3-[(2-hydroxy-2- methylpropyl)amino]propoxy]-N-(3- isoquinolyl)carboxamide

N-((1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-3- hydroxy-3-methylbutyl)-N-(2,2- difluoroethyl){[(2-chloro-3- fluorophenyl)methyl]amino}carboxamide

N-((1S)-3,3-difluoro-4- hydroxy-1-{[N-(5- phenylisoxazol-3- yl)carbamoyloxy]methyl}butyl){[(2-chloro- 3-fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-3,3-difluoro-4-hydroxy-1- {[N-(3-phenylisoxazol-5- yl)carbamoyloxy]methyl}butyl) {[(2-chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide

N-{(1S)-3,3-difluoro-4-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2- chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(1S)-1-({N-[5-(3-fluorophenyl)isoxazol- 3-yl]carbamoyloxy}methyl)-3-hydroxy-3- methylbutyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-((1S)-3-hydroxy-3-methyl-1- {[N-(5-phenylisoxazol-3- yl)carbamoyloxy]methyl}butyl) {[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

(4R)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl acetate

N-{(1R)-4-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl} {[(2,3-difluorophenyl)methyl}amino}-N- methylcarboxamide

(4R)-4-({[(2,3- difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy) pentyl dihydrogen phosphate

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-3-[(2- fluoroethyl)amino]propoxy]-N-(3- isoquinolyl)carboxamide

N-{(1S)-3-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]- 3-methylbutyl}- N-(2,2-difluoroethyl){[(2-chloro-3- fluorophenyl)methyl]amino}carboxamide

N-[(1S)-1-({N-[5-(3-fluorophenyl)isoxazol- 3-yl]carbamoyloxy}methyl)-3-hydroxy-3- methylbutyl]-N-(2,2-difluoroethyl) {[(2-chloro-3- fluorophenyl)methyl]amino}carboxamide

N-[(1S)-3,3-difluoro-1-({N-[3-(3- fluorophenyl)isoxazol-5-yl] carbamoyloxy}methyl)- 4-hydroxybutyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

methyl (4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-{N-[3-(3- fluorophenyl)isoxazol-5- yl]carbamoyloxy}pentanoate

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-3- (1-methylimidazol-4- yl)propoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-3- [(methylsulfonyl)amino]propoxy]-N-(3- isoquinolyl)carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-3- imidazol-4-ylpropoxy]- N-(6-fluoro(3-isoquinolyl))carboxamide

N-{(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-4- [2-(trifluoromethyl)(1,2,4-triazolo[5,1- c]piperazin-7- yl)]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-3- (2-pyridyl)propoxy]-N- (3-isoquinolyl)carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-oxo-5- piperazinylpentyloxy]-N-[3-(3- fluorophenyl)isoxazol-5-yl]carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-oxo-5- piperazinylpentyloxy]-N-[5-(3- fluorophenyl)isoxazol-3-yl]carboxamide

tert-butyl 4-[(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-{N-[3-(3- fluorophenyl)isoxazol-5- yl]carbamoyloxy}pentanoyl] piperazinecarboxylate

N-{(1S)-3-imidazo[1,5- a]piperazin-3-yl-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]propyl} {[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

[(2S)-4-(7-{N-[(2-chloro-3- fluorophenyl)methyl] carbamoyl}imidazo[1,5- a]piperazin-3-yl)-2- (methylamino)butoxy]-N-(3- isoquinolyl)carboxamide

N-[(1S)-3-(7-{N-[(2-chloro-3- fluorophenyl)methyl]carbamoyl} imidazo[1,5-a]piperazin-3-yl)-1- [(N-(3-isoquinolyl)carbamoyloxy) methyl]propyl]{[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

tert-butyl 3-[(3S)-3-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-(N-(3- isoquinolyl)carbamoyloxy) butyl]imidazo[5,1- c]piperazine-7-carboxylate

(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)-N-(pyrazin- 2-ylmethyl)pentanamide

N-{(1S)-3-(4-hydroimidazo[1,5-a] pyrazin-3-yl)-1-[(N-(3-isoquinolyl) carbamoyloxy)methyl] propyl}{[(2-chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-[4- (methylethyl)piperazinyl]-5- oxopentyloxy]-N-(3- isoquinolyl)carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-(9-oxa-3,6- diazabicyclo[4.4.0]dec-3-yl)-5- oxopentyloxy]-N-(3- isoquinolyl)carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- (4-methylpiperazinyl)-5- oxopentyloxy]-N-(3- isoquinolyl)carboxamide

N-{(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]- 4-(1,2,4-triazolo[5,1-c]piperazin- 7-yl)butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-1-[(N-(3-isoquinolyl) carbamoyloxy)methyl]-4-(3- methyl(1,2,4-triazolo[3,4-c]piperazin- 7-yl))butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarboxamide

N-{(1S)-4-(1,1-dioxo(1,4- thiazaperhydroin-4-yl))-1- [(N-(3-isoquinolyl)carbamoyloxy) methyl]butyl}{[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

N-{(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-4-(4- methylpiperazinyl)butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-4- morpholin-4-ylbutyl} {[(2-chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

N-{(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-4- piperazinylbutyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

{[(2-chloro-3- fluorophenyl)methyl]amino}-N-(2-(N- (3-isoquinolyl)carbamoyloxy)-1- {[1-benzylimidazol- 2-yl]methyl}ethyl)-N- methylcarboxamide

{[(2-chloro-3- fluorophenyl)methyl]amino}-N-{2-(N- (3-isoquinolyl)carbamoyloxy)-1- [(1-methylimidazol- 2-yl)methyl]ethyl}-N- methylcarboxamide

{[(2-chloro-3- fluorophenyl)methyl]amino}-N-[1- (imidazol-2-ylmethyl)-2-(N-(3- isoquinolyl)carbamoyloxy)ethyl]-N- methylcarboxamide

N-{(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]- 4-(2-methyl(4,5,6,7- tetrahydroimidazo[5,4-c]pyridin-5- yl))-4-oxobutyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]- 4-[4-(2,2,2-trifluoroethyl) piperazinyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

(3S)-3-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-4-(N-(3- isoquinolyl)carbamoyloxy)-N- (pyrazin-2-ylmethyl)butanamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-3- imidazol-4-ylpropoxy]- N-(3-isoquinolyl)carboxamide

N-{(1S)-2-amino-1-[(N-(3- isoquinolyl)carbamoyloxy) methyl]ethyl}{[(2-chloro- 3-fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(1S)-1-(4-hydroimidazo[1,5- a]pyrazin-3-ylmethyl)-2-(N-(3- isoquinolyl)carbamoyloxy)ethyl] {[(2-chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

N-{(1S)-4-(4-acetylpiperazinyl)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2- chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-4-(3-fluoropiperidyl)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2- chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide

{N-[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3- isoquinolyl)carbamoyloxy)propyl] carbamoyloxy}ethyl acetate

N-{(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-4-(2- oxopiperazinyl)butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(1S)-4-amino-3,3-difluoro-1-({N-[5- (3-fluorophenyl)isoxazol-3- yl]carbamoyloxy}methyl)butyl]{[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

N-[(1S)-5-diazo-3,3-difluoro-1-({N-[5- (3-fluorophenyl)isoxazol-3- yl]carbamoyloxy}methyl)- 5-azapent-5-enyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(1S)-5-diazo-3,3-difluoro-1-({N-[3-(3- fluorophenyl)isoxazol-5- yl]carbamoyloxy}methyl)- 5-azapent-5-enyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(1S)-4-amino-3,3-difluoro-1-({N-[3-(3- fluorophenyl)isoxazol-5- yl]carbamoyloxy}methyl)butyl]{[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

N-[(1S)-1-(imidazo[1,5- a]piperazin-3-ylmethyl)-2- (N-(3-isoquinolyl)carbamoyloxy) ethyl]{[(2-chloro- 3-fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(1S)-1-({N-[3-(3-fluorophenyl)isoxazol- 5-yl]carbamoyloxy}methyl)-3-hydroxy-3- methylbutyl]{[(2-chloro-3-fluorophenyl) methyl]amino}-N-methylcarboxamide

[(2S)-3-[(2,2-difluoroethyl)amino]-2- ({[(2-chloro-3-fluorophenyl)methyl]amino}- N-methylcarbonylamino)propoxy]-N-[5-(3- fluorophenyl)isoxazol-3-yl]carboxamide

[(2S)-3-[(2,2-difluoroethyl)amino]-2- ({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-(5- phenylisoxazol-3-yl)carboxamide

[(2S)-3-[(2,2-difluoroethyl)amino]-2- ({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-[3-(3- fluorophenyl)isoxazol-5-yl]carboxamide

[(2S)-3-[(2,2-difluoroethyl)amino]-2- ({[(2-chloro-3-fluorophenyl)methyl]amino}- N-methylcarbonylamino)propoxy]-N-(3- phenylisoxazol-5-yl)carboxamide

[(2S)-3-(N-(2,2-difluoroethyl){[(2-chloro-3- fluorophenyl)methyl]amino}carbonylamino)- 2-({[(2-chloro-3-fluorophenyl)methyl] amino}-N- methylcarbonylamino)propoxy]-N-[3- (3-fluorophenyl)isoxazol-5-yl]carbo

[(2S)-3-(N-(2,2-difluoroethyl){[(2-chloro-3- fluorophenyl)methyl]amino}carbonylamino)-2- ({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-(3- phenylisoxazol-5-yl)carboxamide

[(2S)-3-(N-(2,2-difluoroethyl){[(2-chloro-3- fluorophenyl)methyl]amino}carbonylamino)-2- ({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-[5-(3- fluorophenyl)isoxazol-3-yl]carbo

[(2S)-3-(N-(2,2-difluoroethyl){[(2-chloro-3- fluorophenyl)methyl]amino}carbonylamino)-2- ({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-(5- phenylisoxazol-3-yl)carboxamide

N-[(1R,2R)-2-(N-(3- isoquinolyl)carbamoyloxy) cyclohexyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N- ethylcarboxamide

N-[(1S)-2-amino-1-({N-[5-(3- fluorophenyl)isoxazol- 3-yl]carbamoyloxy}methyl)ethyl] {[(2-chloro-3-fluorophenyl) methyl]amino}-N-methylcarboxamide

{[(2-chloro-3-fluorophenyl)methyl]amino}- N-[2-(N- (3-isoquinolyl)carbamoyloxy)ethyl]-N- methylcarboxamide

N-[(1S,2S)-2-(N-(3- isoquinolyl)carbamoyloxy)cyclohexyl] {[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(2S,1R)-2-(N-(3-isoquinolyl)carbamoyloxy) cyclopentyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-[(1S,2S)-2-(N-(3-isoquinolyl)carbamoyloxy) cyclopentyl]{[(2-chloro- 3-fluorophenyl)methyl]amino}-N- methylcarboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-3-[(2- hydroxyethyl)amino]propoxy]-N-(3- isoquinolyl)carboxamide

[(2S)-3-[bis(2- hydroxyethyl)amino]-2-({[(2-chloro- 3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-(3- isoquinolyl)carboxamide

[2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-[1- (trifluoromethyl)(3- isoquinolyl)]carboxamide

[2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-[4- (trifluoromethyl)(3- isoquinolyl)]carboxamide

[(2S)-3-amino-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-(5- phenylisoxazol-3-yl)carboxamide

[(2S)-3-amino-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]- N-(4-iodo-5-phenylisoxazol-3- yl)carboxamide

[(2S)-3-amino-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-[5-(3- fluorophenyl)-4-iodoisoxazol-3- yl]carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-[4- (methylethyl)piperazinyl]-5- oxopentyloxy]-N-[5-(3- fluorophenyl)isoxazol-3-yl]carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-[4- (methylethyl)piperazinyl]-5- oxopentyloxy]-N-(5- phenylisoxazol-3-yl)carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-[4- (methylethyl)piperazinyl]-5- oxopentyloxy]-N-[3-(3- fluorophenyl)isoxazol-5-yl]carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- (4-methylpiperazinyl)-5- oxopentyloxy]-N-[3-(3- fluorophenyl)isoxazol-5- yl]carboxamide

[3-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2- methylpropoxy]-N-(3- isoquinolyl)carboxamide

N-{(2S,1R)-2-[(N-(3-isoquinolyl) carbamoyloxy)methyl]cyclopropyl}{[(2- chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide

[((2S)-1-{N-[(2-chloro-3- fluorophenyl)methyl] carbamoyl}pyrrolidin-2- yl)methoxy]-N-[3-(3- fluorophenyl)isoxazol-5- yl]carboxamide

{[(2-chloro-3- fluorophenyl)methyl]amino}-N-[2-(N- (3-isoquinolyl)carbamoyloxy)-1- methylpropyl]-N- methylcarboxamide

{[(2-chloro-3- fluorophenyl)methyl]amino}- N-[2-(N-(3-isoquinolyl) carbamoyloxy)-1- methylpropyl]carboxamide

N-((1S)-3-{3-[(dimethylamino)methyl](1,2,4- oxadiazol-5-yl)}-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]propyl) {[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarboxamide

N-{(1S)-4-(4-ethylpiperazinyl)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-4- oxobutyl}{[(2- chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]- 4-oxo-4-(4-propylpiperazinyl) butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy) methyl]-4-[4-(2-methylpropyl)piperazinyl]- 4-oxobutyl}{[(2-chloro- 3-fluorophenyl)methyl]amino}-N- methylcarboxamide

N-{(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-3-(3- methyl(1,2,4-oxadiazol-5-yl))propyl} {[(2-chloro-3-fluorophenyl) methyl]amino}-N-methylcarboxamide

N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy) methyl]-4-[4-(2,2,2-trifluoroethyl) (1,4-diazaperhydroepinyl)]butyl}{[(2- chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5-[4- (methylethyl)piperazinyl]-5- oxopentyloxy]-N-(3- phenylisoxazol-5-yl)carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- (4-methylpiperazinyl)-5- oxopentyloxy]-N-[5-(3- fluorophenyl)isoxazol-3- yl]carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- (4-methylpiperazinyl)-5- oxopentyloxy]-N-(5-phenylisoxazol-3- yl)carboxamide

N-((1S)-2-amino-1-{[N-(5-chloro(2- pyridyl))carbamoyloxy]methyl} ethyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarboxamide

[5-((3R)-3-methylpiperazinyl)(2S)-2- ({[(2-chloro- 3-fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- oxopentyloxy]-N-(3- isoquinolyl)carboxamide

[(2S)-5-((3S)-3-methylpiperazinyl)-2- ({[(2-chloro- 3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-oxopentyloxy]- N-(3-isoquinolyl)carboxamide

[(2S)-5-((2S)-2-methylpiperazinyl)-2- ({[(2-chloro-3-fluorophenyl)methyl]amino}- N-methylcarbonylamino)-5- oxopentyloxy]-N-(3- isoquinolyl)carboxamide

[5-((2R)-2-methylpiperazinyl)(2S)-2- ({[(2-chloro-3-fluorophenyl) methyl]amino}-N- methylcarbonylamino)-5- oxopentyloxy]-N-(3- isoquinolyl)carboxamide

[(2S)-5-(3,5-dimethylpiperazinyl)-2- ({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-oxopentyloxy]- N-(3-isoquinolyl)carboxamide

[(2S)-5-((3S,5R)-3,5- dimethylpiperazinyl)-2-({[(2- chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-oxopentyloxy]- N-(3-isoquinolyl)carboxamide

[(2S)-2-({[(2-chloro-3-fluorophenyl) methyl]amino}-N-methylcarbonylamino)- 5-(4-cyclopropylpiperazinyl)-5- oxopentyloxy]- N-(3-isoquinolyl)carboxamide

[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(4- cyclobutylpiperazinyl)- 5-oxopentyloxy]-N-(3- isoquinolyl)carboxamide

N-[(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3- isoquinolyl)carbamoyloxy)propyl]-3- hydroxy-2- (hydroxymethyl)-2-methylpropanamide

N-[(1S)-2-amino-1-({N-[3-(3- chlorophenyl)isoxazol-5-yl] carbamoyloxy}methyl)ethyl]{[(2-chloro- 3-fluorophenyl)methyl]amino}-N- methylcarboxamide

[(2S)-5-(3,3-dimethylpiperazinyl)-2- ({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5- oxopentyloxy]-N-(3- isoquinolyl)carboxamide

[(2S)-5-[(2S)-2- (trifluoromethyl)piperazinyl]-2- ({[(2-chloro-3-fluorophenyl) methyl]amino}-N-methylcarbonylamino)- 5-oxopentyloxy]-N-(3- isoquinolyl)carboxamide

N-((1S)-2-{N-[3-(3-chlorophenyl)isoxazol-5- yl]carbamoyloxy}-1-{[(phenylmethoxy) carbonylamino]methyl}ethyl) {[(2-chloro-3-fluorophenyl)methyl] amino}-N-methylcarboxamide and pharmaceutically acceptable salts thereof.

Also provided is at least one chemical entity selected from

-   N-{(1S)-5-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]pentyl}{[(2-chloro-4-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-3,4-dihydroxybutyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   N-((1S,3S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-3,4-dihydroxybutyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   N-((1S,3R)-1-{[N-(6-fluoro(3-isoquinoly))carbamoyloxy]methyl}-3,4-dihydroxybutyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]pentyl]-2-aminoacetamide; -   (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2-hydroxypentyl     dihydrogen phosphate; -   N-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-3-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]propyl]-2-aminoacetamide; -   N-{(1S)-4-amino-1-[(N-pyridino[4,3-d]pyridin-3-ylcarbamoyloxy)methyl]butyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-4-oxo-4-piperazinylbutyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   N-(4-[((1E)-1-amino-2-carbamoyl-2-azavinyl)amino](1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   N-[(1S)-4-amino-1-({N-[5-(trifluoromethyl)(2-pyridyl)]carbamoyloxy}methyl)butyl]{[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)-6-(N-(3-isoquinolyl)carbamoyloxy)hexyl     dihydrogen phosphate; -   [(2S)-5-amino-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)pentyloxy]-N-(5-chloro(2-pyridyl))carboxamide; -   N-((1S)-4-amino-3,3-difluoro-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}butyl)     {[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   [(2S,4R)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(3-isoquinolyl)carboxamide; -   [(2S,4S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(3-isoquinolyl)carboxamide; -   [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-oxo-5-piperazinylpentyloxy]-N-(3-isoquinolyl)carboxamide; -   N-{(1S,3S)-3,4-dihydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]butyl}{[(2,3-difluorophenyl)methyl]amino}-N-methylcarboxamide; -   N-{(1S,3R)-3,4-dihydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]butyl}{[(2,3-difluorophenyl)methyl]amino}-N-methylcarboxamide; -   (4S,2R)-4-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)-2-hydroxy-5-(N-(3-isoquinolyl)carbamoyloxy)pentyl     dihydrogen phosphate; -   (2S,4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)-2-hydroxy-5-(N-(3-isoquinolyl)carbamoyloxy)pentyl     dihydrogen phosphate; -   N-{(1S)-4-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]butyl}{[(2,3-difluorophenyl)methyl]amino}-N-methylcarboxamide; -   (4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)pentyl     dihydrogen phosphate; -   [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-hydroxy-4,4-dimethylpentyloxy]-N-(6-fluoro(3-isoquinolyl))carboxamide; -   (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2,2-dimethylpentyl     dihydrogen phosphate; -   N-((1S,3R)-3,4-dihydroxy-1-{[N-(3-phenylisoxazol-5-yl)carbamoyloxy]methyl}butyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   (4S,2R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-2-hydroxy-5-(N-(3-isoquinolyl)carbamoyloxy)pentyl     dihydrogen phosphate; -   (4S,2R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-2-hydroxy-5-[N-(3-phenylisoxazol-5-yl)carbamoyloxy]pentyl     dihydrogen phosphate; -   N-{(1S)-1-[(N-benzothiazol-2-ylcarbamoyloxy)methyl]-4-oxo-4-piperazinylbutyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   N-{(1S)-1-[((2S)-2,3-dihydroxypropoxy)methyl]-2-(N-(3-isoquinolyl)carbamoyloxy)ethyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   (2R)-3-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-3-(N-(3-isoquinolyl)carbamoyloxy)propoxy]-2-hydroxypropyl     dihydrogen phosphate; -   N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-(1,2,4-triazolo[3,4-c]piperazin-7-yl)butyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-3-imidazol-4-ylpropoxy]-N-(6-fluoro(3-isoquinolyl))carboxamide; -   [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-3-(2-pyridyl)propoxy]-N-(3-isoquinolyl)carboxamide; -   [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-oxo-5-piperazinylpentyloxy]-N-[3-(3-fluorophenyl)isoxazol-5-yl]carboxamide; -   [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-oxo-5-piperazinylpentyloxy]-N-[5-(3-fluorophenyl)isoxazol-3-yl]carboxamide; -   [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-[4-(methylethyl)piperazinyl]-5-oxopentyloxy]-N-(3-isoquinolyl)carboxamide; -   N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-(4-methylpiperazinyl)butyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-(2-methyl(4,5,6,7-tetrahydroimidazo[5,4-c]pyridin-5-yl))-4-oxobutyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-(2-oxopiperazinyl)butyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   N-[(1S)-4-amino-3,3-difluoro-1-({N-[3-(3-fluorophenyl)isoxazol-5-yl]carbamoyloxy}methyl)butyl]{[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide; -   N-[(1S)-1-(imidazo[1,5-a]piperazin-3-ylmethyl)-2-(N-(3-isoquinolyl)carbamoyloxy)ethyl]{[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide;     and -   [(2S)-3-[(2,2-difluoroethyl)amino]-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)propoxy]-N-[3-(3-fluorophenyl)isoxazol-5-yl]carboxamide,     and pharmaceutically acceptable salts thereof.

Many of the optionally substituted starting compounds and other reactants are commercially available, e.g. from Aldrich Chemical Company (Milwaukee, Wis.) or can be readily prepared by those skilled in the art using commonly employed synthetic methodology.

The chemical entities described herein can be synthesized utilizing techniques well known in the art from commercially available starting materials and reagents. For example, the chemical entities described herein can be prepared as illustrated below with reference to the examples and reaction schemes.

Unless specified to the contrary, the reactions described herein take place at atmospheric pressure, generally within a temperature range from −10° C. to 200° C. Further, except as employed in the examples or as otherwise specified, reaction times and conditions are intended to be approximate, e.g. taking place at about atmospheric pressure within a temperature range of about −10° C. to about 110° C. over a period of about 1 to about 24 hours; reactions left to run overnight average a period of about 16 hours. For each gram of the limiting reagent, one cc (or mL) of solvent constitutes a volume equivalent.

The terms “solvent,” “organic solvent,” and “inert solvent” each mean a solvent inert under the conditions of the reaction being described in conjunction therewith [including, for example, benzene, toluene, acetonitrile, tetrahydrofuran (“THF”), dimethylformamide (“DMF”), chloroform, methylene chloride (or dichloromethane), diethyl ether, methanol, N-methylpyrrolidone (“NMP”), pyridine and the like]. Unless specified to the contrary, the solvents used in the reactions described herein are inert organic solvents. Unless specified to the contrary, for each gram of the limiting reagent, one cc (or mL) of solvent constitutes a volume equivalent.

Isolation and purification of the compounds and intermediates described herein can be effected, if desired, by any suitable separation or purification procedure such as, for example, filtration, extraction, crystallization, column chromatography, thin-layer chromatography or thick-layer chromatography, or a combination of these procedures. Specific illustrations of suitable separation and isolation procedures can be had by reference to the examples hereinbelow. However, other equivalent separation or isolation procedures can also be used.

When desired, the (R) and (S) isomers may be resolved by methods known to those skilled in the art, for example by formation of diastereoisomeric salts or complexes which may be separated, for example, by crystallization; via formation of diastereoisomeric derivatives which may be separated, for example, by crystallization, gas-liquid or liquid chromatography; selective reaction of one enantiomer with an enantiomer-specific reagent, for example enzymatic oxidation or reduction, followed by separation of the modified and unmodified enantiomers; or gas-liquid or liquid chromatography in a chiral environment, for example on a chiral support, such as silica with a bound chiral ligand or in the presence of a chiral solvent. It will be appreciated that when the desired enantiomer is converted into another chemical entity by one of the separation procedures described above, a further step may be required to liberate the desired enantiomeric form. Alternatively, a specific enantiomer may be synthesized by asymmetric synthesis using optically active reagents, substrates, catalysts and/or solvents, or by converting one enantiomer to the other by asymmetric transformation.

The chemical entities described herein may be useful in a variety of applications involving smooth muscle cells and/or non-muscle cells. In certain embodiments, the chemical entities may be used to inhibit smooth muscle myosin. The chemical entities may be useful to bind to, and/or inhibit the activity of, smooth muscle myosin. In certain embodiments, the smooth muscle myosin is human, although the chemical entities may be used to bind to or inhibit the activity of smooth muscle myosin from other organisms, such as other mammals.

In certain embodiments, the chemical entities may be used to inhibit non-muscle myosin. The chemical entities may be useful to bind to, and/or inhibit the activity of, non-muscle myosin. In certain embodiments, the non-muscle myosin is human, although the chemical entities may be used to bind to or inhibit the activity of non-muscle myosin from other organisms, such as other mammals.

The chemical entities described herein may be used to treat disease states associated with smooth muscle and/or non-muscle myosin. Such disease states which can be treated by the chemical entities described herein include, but are not limited to, hypertension, asthma, incontinence, chronic obstructive pulmonary disorder, pre-term labor, and the like. It is appreciated that in some cases the cells may not be in an abnormal state and still require treatment. Other disease states which may be treated by the chemical entities described herein include, but are not limited to, systemic hypertension, chronic heart failure, migraine and outpatient treatment of angina, pulmonary hypertension, perioperative hypertension, hypertensive emergency, cerebral vasospasm after cerebrovascular hemorrhage, in-hospital treatment of angina (including atypical angina) and/or acute heart failure. Additional disease states which may be treated include, but are not limited to, Also bronchospasm, asthma, cardiovascular, cerebrovascular and peripheral vascular diseases, vasospasm after cerebrovascular hemorrhage, erectile dysfunction, gastrointestinal motility dysfunction (e.g., irritable bowel syndrome), overactive bladder/stress urinary incontinence, and preterm labor.

Thus, in certain embodiments, the chemical entities described herein are applied to cells or administered to individuals afflicted or subject to impending affliction with any one of these disorders or states.

More specifically, the chemical entities described herein may be useful for the treatment of diseases or symptoms related to abnormal increased muscle tone or excessive contraction, or spasm of vascular smooth muscle in systemic, coronary, pulmonary circulation, and micro-circulatory smooth muscle as well, such as systemic hypertension, malignant hypertension, hypertension crisis, symptomatic hypertension, pulmonary hypertension, pulmonary infarction, angina pectoris, cardiac infarction, micro-circulation malfunction under shock condition, and infarction occurred in other location or organs of the human or animal body. Other diseases or symptoms that can be treated with the chemical entities described herein include:

spasm of gastro-intestine smooth muscle, including sphincters, such as gastric spasm, pylorospasm, and spasms of biliary tract, pancreatic tract, urinary tract, caused by inflammation, stimulation of stones or parasites;

spasm of other visceral organs such as uterus, Fallopian tube, and so on;

spasm of trachea-bronchial tree smooth muscle, diaphragm muscle, such as various asthma, breathlessness, dyspnea, diaphragmatic convulsion, and so on;

spasm of alimentary canal smooth muscle, including stomach, intestine and colons, biliary and pancreatic duct etc.; and

spasm of urinary tract smooth muscle.

In addition, the chemical entities described herein can be used for control, management and manipulation of labor during pregnancy. The method is particularly useful for inhibition of spontaneous preterm labor which would, if untreated, result in premature delivery or abortion and for inhibition of surgically induced labor during transuterine fetal surgery. The method is also useful for inducing the labor in overterm pregnancies where the labor does not occur on term and when it is necessary to induce labor in order to assure the normal delivery.

Further, the chemical entities described herein can be used for the treatment of “airway wall remodeling”, which is a condition associated with diseases or conditions characterized by airway wall thickening and air obstruction, which may, for example, occur in the small airways of patients with certain respiratory disease conditions, such as chronic obstructive pulmonary disease (COPD).

Such disease states which can be treated by the chemical entities, compositions and methods provided herein also include, but are not limited to glaucoma and other ocular indications. More specifically, chemical entities described herein may be useful for the treatment of diseases or symptoms related to glaucoma, including increased intraocular pressure, reduced flow of intraocular aqueous humor, and optical nerve damage. Other diseases or symptoms that can be treated with the chemical entities, compositions, and methods described herein including intraocular hypertenstion.

ATP hydrolysis is employed by myosin to produce force. An increase in ATP hydrolysis would correspond to an increase in the force or velocity of muscle contraction. In the presence of actin, myosin ATPase activity is stimulated more than 100-fold. Thus, the measurement of ATP hydrolysis not only measures myosin enzymatic activity but also its interaction with the actin filament. Assays for such activity may employ smooth muscle myosin from a human source, although myosin from other organisms can also be used. Systems that model the regulatory role of calcium in myosin binding may also be used.

The in vitro rate of ATP hydrolysis correlates to smooth muscle myosin potentiating activity, which can be determined by monitoring the production of either ADP or phosphate, for example as described in U.S. Pat. No. 6,410,254. ADP production can also be monitored by coupling the ADP production to NADH oxidation (using, for example, the enzymes pyruvate kinase and lactate dehydrogenase) and monitoring the NADH level, by example, either by absorbance or fluorescence (Greengard, P., Nature 178 (Part 4534): 632-634 (1956); Mol Pharmacol 1970 January; 6(1):31-40). Phosphate production can be monitored using purine nucleoside phosphorylase to couple phosphate production to the cleavage of a purine analog, which results in either a change in absorbance (Proc Natl Acad Sci USA 1992 Jun. 1; 89(11):4884-7) or fluorescence (Biochem J 1990 Mar. 1; 266(2):611-4). While a single measurement is employed, multiple measurements of the same sample at different times in order may be used to determine the absolute rate of the protein activity; such measurements have higher specificity particularly in the presence of test compounds that have similar absorbance or fluorescence properties with those of the enzymatic readout.

Test compounds may be assayed in a highly parallel fashion using multiwell plates by placing the compounds either individually in wells or testing them in mixtures. Assay components including the target protein complex, coupling enzymes and substrates, and ATP may then be added to the wells and the absorbance or fluorescence of each well of the plate can be measured with a plate reader.

One method uses a 384 well plate format and a 25 μL reaction volume. A pyruvate kinase/lactate dehydrogenase coupled enzyme system (Huang T G and Hackney D D. (1994) J Biol Chem 269(23):16493-16501) is used to measure the rate of ATP hydrolysis in each well. As will be appreciated by those of skill in the art, the assay components are added in buffers and reagents. Since the methods outlined herein allow kinetic measurements, incubation periods may be optimized to give adequate detection signals over the background. The assay is performed in real time to give the kinetics of ATP hydrolysis to increase the signal-to-noise ratio of the assay.

Selectivity for smooth muscle myosin may be determined by substituting other myosins in one or more of the above-described assays and comparing the results obtained against those obtained using the cardiac equivalents.

Chemical entities identified by the methods described herein as smooth muscle myosin modulators may be further tested in an efficacy screen, such as a screen using strips of permeabilized smooth muscle from, e.g. chicken gizzard. Calcium-sensitive smooth muscle strips are prepared by dissecting chicken gizzard tissue, followed by treatment with 1% Triton X-100 to make the strips permeable to exogenous compounds (Barsotti, R J, et al., Am J. Physiol. 1987 May; 252(5 Pt 1):C543-54). These strips can be stored in 50% glycerol for several weeks at −20° C., allowing multiple experiments to be performed with each batch of muscle strips. Experiments are performed using a solution of 20 mM imidazole pH 7.0, 5.5 mM ATP, 7 mM MgCl₂, 55 mM KCl, 1 μM Calmodulin, and 10 mM EGTA. Free calcium will be controlled by addition of various amounts of CaCl₂, according to the calculations of MAXChelator (Patton, et al. Cell Calcium. 35/5 pp. 427-431, 2004). An isometric muscle fiber apparatus is used to measure isometric tension, for example using an Aurora Scientific 400 A transducer with National Instruments PCI-MIO-16E-4, 16 channels, 12 bit A/D board for data acquisition. The chemically skinned gizzard fibers are relaxed when bathed in low calcium solutions (pCa 8), but develop isometric tension when the free calcium of the bathing solution is increased to pCa 5. These fibers can be repeatedly contracted and relaxed by switching between high and low calcium bathing solutions.

Compounds are first tested for their ability to prevent contraction of gizzard strips, by preincubating relaxed fibers with a compound, followed by transfer to high calcium solution containing the compound. Next, compounds are tested for their ability to cause relaxation of contracting fibers by adding the compound to fibers already incubating in high calcium solution. Washout experiments are performed to ensure that the inhibitory effects are reversible, so that the compounds do not cause denaturation or other irreparable damage to the smooth muscle myosin.

The chemical entities are administered at a therapeutically effective dosage, e.g. a dosage sufficient to provide treatment of the disease states previously described. Generally, a daily dose is from about 0.05 to about 100 mg/kg of body weight, such as from about 0.10 to about 10 mg/kg of body weight or from about 0.15 to about 1 mg/kg of body weight. Thus, for administration to a 70 kg person, the dosage range is from about 3.5 to about 7000 mg per day, such as from about 7 to about 700 mg per day or from about 10 to about 100 mg per day. The amount of active chemical entity administered will, of course, be dependent on the subject and disease state being treated, the severity of the affliction, the manner and schedule of administration and the judgment of the prescribing physician; for example, a dose range for oral administration may be from about 70 to about 700 mg per day, whereas for intravenous administration the dose range may be from about 700 to about 7000 mg per day. The active agents may be selected for longer or shorter plasma half-lives, respectively.

Administration of the chemical entities described herein including pharmaceutically acceptable salts thereof can be via any of the accepted modes of administration for agents that serve similar utilities including, but not limited to, orally, subcutaneously, intravenously, intranasally, topically, transdermally, sublingually, intramucosally, intraperitoneally, intramuscularly, intrapulmonarilly, vaginally, rectally, and intraocularly (including intraocular injection). Oral, topical, parenteral, and intraocular administration are customary in treating many of the indications recited herein.

Pharmaceutically acceptable compositions include solid, semi-solid, liquid and aerosol dosage forms, such as, e.g. tablets, capsules, powders, liquids, suspensions, suppositories, aerosols, and the like. The chemical entities can also be administered in sustained- or controlled-release dosage forms, including depot injections, osmotic pumps, pills, transdermal (including electrotransport) patches, drops and the like, for prolonged and/or timed, pulsed administration at a predetermined rate. The compositions may be provided in unit dosage forms suitable for single administration of a precise dose.

The chemical entities may be administered either alone or in combination with a conventional pharmaceutical carrier or the like (e.g. mannitol, lactose, starch, magnesium stearate, sodium saccharine, talcum, cellulose, sodium crosscarmellose, glucose, gelatin, sucrose, magnesium carbonate, and the like). If desired, the pharmaceutical composition may also contain minor amounts of nontoxic auxiliary substances such as wetting agents, emulsifying agents, solubilizing agents, pH buffering agents and the like (e.g. sodium acetate, sodium citrate, cyclodextrine derivatives, sorbitan monolaurate, triethanolamine acetate, triethanolamine oleate. Generally, depending on the intended mode of administration, the pharmaceutical composition may contain from about 0.005% to about 95%, for example, from about 0.5% to about 50%, by weight of at least one chemical entity described herein. Actual methods of preparing such dosage forms are known or will be apparent, to those skilled in this art; for example, see Remington's Pharmaceutical Sciences, Mack Publishing Company, Easton, Pa. Pharmaceutical compositions are also referred to as pharmaceutical formulations.

In addition, the chemical entities may be co-administered with, and the pharmaceutical compositions can include, other medicinal agents, pharmaceutical agents, adjuvants, and the like.

In certain embodiments, the compositions are in the form of a pill or tablet and contain, along with the active ingredient, one or more of a diluent such as lactose, sucrose, dicalcium phosphate, and the like; a lubricant such as magnesium stearate or the like; and a binder such as starch, gum acacia, polyvinylpyrrolidine, gelatin, cellulose, cellulose derivatives and the like. In another solid dosage form, a powder, marume, solution or suspension (e.g. in propylene carbonate, vegetable oils or triglycerides) may be encapsulated in a gelatin capsule.

Liquid pharmaceutical compositions may, for example, be prepared by dissolving, dispersing, etc. at least one chemical entity and one or more optional pharmaceutical adjuvants in a carrier (e.g. water, saline, aqueous dextrose, glycerol, glycols, ethanol and the like) to form a solution or suspension. Injectables may be prepared in conventional forms, either as liquid solutions or suspensions, as emulsions, or in solid forms suitable for dissolution or suspension in liquid prior to injection. The percentage of chemical entities contained in such parenteral compositions is highly dependent on the specific nature thereof, as well as the activity of the chemical entities and the needs of the subject. However, percentages of active ingredient ranging from about 0.01% to about 10% in solution may be used, and may be higher if the composition is a solid which will be subsequently diluted to the above percentages. In certain embodiments, the composition has from about 0.2% to about 2% of the active agent in solution.

Compositions comprising at least one chemical entity may be administered intraocularly (including intraocular, periocular, and retrobulbar injection and perfusion). When administered intraocularly the sterile composition is typically aqueous. An appropriate buffer system may be added to prevent pH drift under storage conditions. When administered during intraocular surgical procedures, such as retrobulbar or periocular injection and intraocular perfusion or injection, the use of balanced salt irrigating solutions may be necessary. When used in a multidose form, preservatives may be required to prevent microbial contamination during use.

Compositions comprising at least one chemical entity may also be administered topically as eye drops, eye wash, creams, ointments, gels, and sprays. When administered as eye drops or eye wash, the active ingredients are typically dissolved or suspended in suitable carrier, typically a sterile aqueous solvent. An appropriate buffer system may be added to prevent pH drift under storage conditions. When used in a multidose form, preservatives may be required to prevent microbial contamination during use.

Compositions comprising at least one chemical entity may also be administered to the respiratory tract as an aerosol or in a solution for a nebulizer, or as a microfine powder for insufflation, alone or in combination with an inert carrier such as lactose. The particles of the composition typically have diameters of less than 50 microns, for example, less than 10 microns.

Packaged pharmaceutical compositions comprising a pharmaceutical composition described herein and instructions for using the composition to treat a patient suffering from a disease associated with smooth muscle myosin or non-muscle myosin. The packaged pharmaceutical compositions described herein are also used to treat a patients suffering from a disease associated with smooth muscle myosin selected from hypertension, asthma, chronic obstructive pulmonary disease, bronchoconstrictive disease, glaucoma and other ocular indications, incontinence and other bladder disfunctions, irritable bowel syndrome, pre-term labor, esophogial dysmotility, strokes, subarachnoid hemmorhages, pre-menstrual cramps, erectile dysfunction and other acute and chronic diseases and conditions associated with smooth muscle myosin and/or non-muscle myosin.

Also provided is a method of treating or ameliorating a disease associated with smooth muscle myosin or non-muscle myosin in a mammal which method comprises administering to a mammal in need thereof a therapeutically effective amount of at least one chemical entity described herein.

In some embodiments, the method of treating or ameliorating a disease associated with smooth muscle myosin or non-muscle myosin described herein is used to treat diseases selected from hypertension, asthma, chronic obstructive pulmonary disease (COPD), bronchoconstrictive disease, glaucoma and other ocular indications, incontinence and other bladder disfunctions, irritable bowel syndrome, pre-term labor, esophogial dysmotility, strokes, subarachnoid hemmorhages, pre-menstrual cramps, erectile dysfunction and other acute and chronic diseases and conditions associated with smooth muscle myosin and/or non-muscle myosin.

Also provided is a method of treating or ameliorating a disease associated with airway wall remodeling in a mammal which method comprises administering to a mammal in need thereof a therapeutically effective amount of at least one chemical entity described herein.

Generally, to employ the chemical entities described herein in methods of screening for smooth muscle myosin binding, smooth muscle myosin is bound to a support and at least one chemical entity is added to the assay. Alternatively, the chemical entity may be bound to the support and the smooth muscle myosin added. Classes of compounds among which novel binding agents may be sought include specific antibodies, non-natural binding agents identified in screens of chemical libraries, peptide analogs, etc. Of particular interest are screening assays for candidate agents that have a low toxicity for human cells. A wide variety of assays may be used for this purpose, including labeled in vitro protein-protein binding assays, electrophoretic mobility shift assays, immunoassays for protein binding, functional assays (phosphorylation assays, etc.), and the like. See, e.g. U.S. Pat. No. 6,495,337.

I. EXAMPLES

The following examples serve to more fully describe the manner of using the invention. These examples are presented for illustrative purposes and should not serve to limit the true scope of the invention.

Example 1 Preparation of 6-fluoro-isoquinoline-3-carbonyl azide

To a suspension of 3-fluoro-DL-phenylalanine (100 g) in conc. HCl (1.0 L) was added aq. formaldehyde solution (37% wt.; 400 mL). The reaction mixture was heated to 90° C. and stirred for 3.5 h, then cooled to RT and stirred overnight and filtered. The filtrate was concentrated and the residue was combined with the precipitate to give 6-fluoro-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, which was used without further purification. LRMS (M+H⁺) m/z 196.1.

To a suspension of 6-fluoro-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid in methanol (500 mL) was added SOCl₂ (50 mL). The reaction mixture was then refluxed for 1 h until LC-MS indicated the completion of the reaction. The mixture was concentrated, and the resulting residue was dissolved in a mixture of EtOAc (1 L) and sat. sodium bicarbonate solution (500 mL). The organic layer was separated, washed with water and brine, dried over Na₂SO₄, and concentrated under reduced pressure to give 6-fluoro-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid methyl ester as an oil (92 g). LRMS (M+H⁺) m/z 210.1.

A mixture of 6-fluoro-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid methyl ester (92 g) and sulfur (42 g, 3 equiv.) in xylene (5 L) was stirred at 150° C. for 16 h. The reaction mixture was concentrated, and the resulting residue was dissolved in EtOAc, which was washed with water and brine, dried over Na₂SO₄, and concentrated under reduced pressure to give a crude mixture. Purification by flash column chromatography (hexanes/EtOAc, gradient 50%-100%) gave 6-fluoro-isoquinoline-3-carboxylic acid methyl ester as a light yellow solid (27 g, 24% for 3 steps). LRMS (M+H⁺) m/z 206.1.

A solution of 6-fluoro-isoquinoline-3-carboxylic acid methyl ester (27 g) and hydrazine (42 g, 10 equiv.) in ethanol (500 mL) was refluxed for 2 h. The reaction mixture was concentrated under high vacuum to remove hydrazine, and the resulting residue was triturated with ethanol (100 mL) to give 6-fluoro-isoquinoline-3-carboxylic acid hydrazide as a light yellow solid (22.8 g, 84%). LRMS (M+H⁺) m/z 206.1.

To a suspension of 6-fluoro-isoquinoline-3-carboxylic acid hydrazide in HCl (1 N, 50 mL) and water (1 L) was added a solution of NaNO₂ (11.4 g, 170 mmol, 1.5 eq) in water (100 mL) dropwise at 0-5° C. The mixture was stirred at 0-5° C. for 1 h. Another solution of NaNO₂ (5.7 g, 85 mmol, 0.5 equiv.) in water (30 mL) was added and the reaction was stirred at 0-5° C. for 3 h until LC-MS indicated the completion of the reaction. The precipitate was filtered, washed with cold water, and dried under high vacuum to give 6-fluoro-isoquinoline-3-carbonyl azide as a light yellow solid (21.3 g, 89%). LRMS (M+H⁺) m/z 217.1.

Example 2 Preparation of benzo[d]thiazole-2-carbonyl azide

To a solution of ethyl benzo[d]thiazole-2-carboxylate (10 g, 48.25 mmol) in ethanol (200 mL) was added hydrazine (15.5 g, 482.5 mmol). The reaction mixture was stirred at RT for 30 min and concentrated under high vacuum to remove hydrazine. The resulting residue was triturated with ethanol (40 mL) to give benzo[d]thiazole-2-carbohydrazide (9.3 g, quant.) LRMS (M+H⁺) m/z 194.0.

To a suspension of benzo[d]thiazole-2-carbohydrazide (9.3 g, 48.2 mmol) in aqueous HCl (1 N, 75 mL, 75 mmol) and water (200 mL) was added a solution of NaNO₂ (6.9 g, 100 mmol) in water (50 mL) dropwise at 0-5° C. The mixture was stirred at 0-5° C. for 2 h and RT for 2 h. The precipitate was filtered, washed with cold water, and dried under high vacuum to give benzo[d]thiazole-2-carbonyl azide (9.0 g, 92%). LRMS (M+H⁺) m/z 205.1.

Example 3 Preparation of isoquinoline-3-carbonyl azide

To a solution of methyl isoquinoline-3-carboxylate (10 g, 53.42 mmol) in ethanol (100 mL) was added hydrazine (17.1 g). The reaction mixture was refluxed for 30 min and concentrated under high vacuum to remove hydrazine. The resulting residue was triturated with ethanol (20 mL) to give isoquinoline-3-carbohydrazide (8.6 g, 86%). LRMS (M+H⁺) m/z 188.1.

To a suspension of isoquinoline-3-carbohydrazide (43 g, 0.23 mol) in aqueous HCl (1 N, 230 mL) and water (1 L) was added a solution of NaNO₂ (23.8 g, 0.34 mol) in water (200 mL) dropwise at 0-5° C. The mixture was stirred at 0-5° C. for 4 h. LC-MS indicated the reaction was not completed. Another solution of NaNO₂ (11.9 g, 0.115 mol) in water (60 mL) was added and the reaction mixture was stirred at 0-5° C. until LC-MS indicated the completion of the reaction. The precipitate was filtered, washed with cold water, and dried under high vacuum to give isoquinoline-3-carbonyl azide (42.7 g, 93.8%) as a white solid. LRMS (M+H⁺) m/z 199.2.

Example 4 Preparation of 5-(3-fluorophenyl)isoxazole-3-carbonyl azide

To a solution of 3-fluoro-acetophenone (27.6 g, 200 mmol, 1.0 equiv.) in DMF (400 mL) at 0° C. was added NaH (8.8 g, 220 mmol, 1.1 equiv.) in two portions over 10 min, followed by diethyloxalate (29.8 mL, 220 mmol, 1.1 equiv.) in 20 min. The mixture was stirred for 15 min, then poured to a mixture of ice and saturated NH₄C1 solution (500 mL). The mixture was extracted with EtOAc (400 mL×3). The organic layers were combined, dried over MgSO₄, and concentrated. The residue was purified by flash column chromatography (hexane/EtOAc, gradient 0% to 40%) to give ethyl 4-(3-fluorophenyl)-2,4-dioxobutanoateas a brownish solid (30 g, 63%). LRMS (M+H⁺) m/z 239.0.

To a solution of ethyl 4-(3-fluorophenyl)-2,4-dioxobutanoate (30.0 g, 126 mmol) in EtOH (300 mL) was added hydroxylamine hydrogen chloride (17 g, 252 mmol). The mixture was stirred at 80° C. for 1 h. The mixture was concentrated to 80 mL and diluted with H₂O (100 mL). The precipitate was filtered and washed with H₂O to give ethyl 5-(3-fluorophenyl)isoxazole-3-carboxylate (25.8 g, 87%). LRMS (M+H⁺) m/z 236.0.

To a solution of ethyl 5-(3-fluorophenyl)isoxazole-3-carboxylate (25.8 g, 110 mmol, 1.0 equiv.) in EtOH (300 mL), was added hydrazine (10.5 mL, 330 mmol, 3.0 equiv.). The mixture was stirred at 80° C. for 1 h and then cooled to RT The precipitate was filtered, washed with H₂O, and dried in vacuum to give 5-(3-fluorophenyl)isoxazole-3-carbohydrazide (20 g). The filtrate was concentrated and the resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give desired product (2.5 g). LRMS (M+H⁺) m/z 222.0.

To a suspension of 5-(3-fluorophenyl)isoxazole-3-carbohydrazide (22.5 g, 101 mmol) in H₂O (2000 mL) and HCl (2 N, 101 mL, 2.0 equiv.) at 0° C. was added a solution of sodium nitrite (13.9 g, 202 mmol, 2.0 equiv.) in H₂O (100 mL). The suspension was stirred at RT for 16 h. The precipitate was filtered and washed with H₂O. The solid was dried under high vacuum to give 5-(3-fluorophenyl)isoxazole-3-carbonyl azide as a yellow solid (20 g, 85%). LRMS (M+H⁺) m/z 179.0.

Example 5 Preparation of 3-(3-fluorophenyl)isoxazole-5-carbonyl azide

A mixture of methyl 3-(3-fluorophenyl)isoxazole-5-carboxylate (prepared according to the literature method: T. T. Dang, U. Albrecht and P. Langer, Preparation 2006, No. 15, 2515-252; or treatment of 3-(3-fluorophenyl)isoxazole-5-carboxylic acid with thionyl chloride and methanol) (5.55 g, 25 mmol, 1.0 equiv.), hydrazine (960 mg, 30 mmol) and MeOH (100 mL) was refluxed for 1 h and concentrated. The residue was washed with dichloromethane and dried in vacuum to give 3-(3-fluorophenyl)isoxazole-5-carbohydrazide (5.6 g, quant.). LRMS (M+H⁺) m/z 222.0

To a suspension of hydrazide (4.33 g, 19.6 mmol, 1.0 equiv.) in H₂O (80 mL) and HCl (1 N, 39.2 mL, 2.0 equiv.) at 0° C. was added a solution of sodium nitrite (2.03 g, 29.4 mmol, 1.5 equiv.) in H₂O (10 mL). The suspension was stirred at RT for 16 h. Then the precipitate was filtered and washed with H₂O until PH=7. The precipitate was dried under high vacuum, which afforded 3-(3-fluorophenyl)isoxazole-5-carbonyl azide as an off white solid (4.0 g, 88%).

Example 6 Preparation of 3-phenylisoxazole-5-carbonyl azide

To a solution of 3-phenylisoxazole-5-carboxylic acid (1.0 g, 5 mmol, 1.0 equiv.) in DMF (20 mL) and THF (20 mL), was added HBTU (2.28 g, 6 mmol, 1.2 equiv.), followed by sodium azide (0.65 g, 10 mmol, 2.0 equiv.) and DIEA (2.6 mL, 15 mmol, 3.0 equiv.). The mixture was stirred at RT for 30 min, concentrated, followed by adding of H₂O (40 mL). The precipitate was filtered, washed with H₂O, and dried in vacuo to give 3-phenylisoxazole-5-carbonyl azide (0.65 g, 60%). LRMS (M−18+H⁺) m/z 187.1.

Example 7 Preparation of (2-chloro-3-fluorophenyl)methanamine hydrochloride

To a solution of NaBH₄ (24.3 g, 0.643 mol) in THF (400 mL) was added TFA (48 mL, 0.643 mol) slowly at 0° C. After the addition was completed, the mixture was stirred at 0° C. for about 20 min. 2-Chloro-3-fluorobenzonitrile (20 g, 0.128 mol) in THF (100 mL) was then added slowly into the mixture at 0° C. The mixture was stirred from 0° C. to RT until no starting material was observed by LCMS. Half of the solvent was removed, then 10% HCl (250 mL) was added slowly into the residue at 0° C. The mixture was warmed up and heated to reflux until no boron complex was observed by LCMS. The mixture was extracted by diethyl ether. The aqueous solution was basified to pH 8-10 using NaOH (3 N), extracted with EtOAc. The organic layers were combined and concentrated to about 300 mL. HCl (4 N, 50 mL) was added slowly into the resulting solution. The white solid was precipitated and collected by filtration to give (2-chloro-3-fluorophenyl)methanamine hydrochloride (21 g, 84%). LRMS (M+H⁺) m/z 160.1.

Example 8 Preparation of 4-nitrophenyl 2-chloro-3-fluorobenzylcarbamate

A 5 liter 3-neck RBF was charged with 4-nitrophenylchloroformate (126.3 g, 627 mmol), DCM (3000 mL), under N₂ atm and chilled in a 0° C. ice bath. A solution of 2-chloro,3-fluorobenzylamine (100.0 g, 627 mmol) followed by solid Sodium Carbonate (155.0 g, 1460 mmol) was quickly added in one portion into the reaction solution. The reaction mixture was stirred at 0° C. for 1 h and an LC/MS was taken to confirm consumption of the starting material and presence of the nitrophenyl intermediate. The reaction mixture was allowed to warm to room temperature and stirred for approximately 2 h. The mixture was filtered, and the filtrate was concentrated to give a white solid. The solid was redissolved with 600 ml of DCM and heated to 40° C. until all of the material went into solution. The solution was chilled in a 0° C. ice bath to form crystals. The crystals were collected and dried under vacuum to give 4-nitrophenyl 2-chloro-3-fluorobenzylcarbamate. (150 g, 75%).

Example 9 Preparation of (2S)-2-((2-chloro-3-fluorobenzyl)(methyl)amino)-4,5-dihydroxypentyl 6-fluoroisoquinolin-3-ylcarbamate

To a solution of (S)-2-aminopent-4-enoic acid (100 g, 0.87 mol), NaOH (2 N, 455 mL) and water (225 mL) in THF (910 mL) was added Boc₂O (199 g, 0.91 mol). The reaction mixture was stirred at RT for 30 h. The reaction mixture was concentrated to remove most of THF. The aqueous solution was washed with 250 mL of EtOAc and acidified to pH3-4 at 0° C. using HCl (2 N, ˜260 mL). The mixture was extracted with EtOAc (350 mL×3), washed with water and brine, dried with Na₂SO₄, and concentrated to give (S)-2-(tert-butoxycarbonylamino)pent-4-enoic acid (185 g), which was used without further purification. LRMS (M+Na⁺) m/z 238.2.

To a solution of (S)-2-(tert-butoxycarbonylamino)pent-4-enoic acid (166 g, 0.77 mol) and Et₃N (214 mL) in THF (2.5 L) was added methyl chloroformate (71.2 mL, 0.93 mol) at 0-5° C. The reaction mixture was stirred for 15 min and filtered to remove TEA salt. To the filtrate was added a solution of NaBH₄ (60 g, 1.54 mol) in a small amount of water at 0-5° C. The reaction was stirred at RT for 1 h and quenched with saturated NH₄Cl solution. The reaction mixture was concentrated to remove most of THF and extracted with EtOAc (700 mL×3). The organic layers were washed with water, NaOH (1 N) and brine, dried over Na₂SO₄, and concentrated to give (S)-tert-butyl 1-hydroxypent-4-en-2-ylcarbamate (165 g), which was used without further purification. LRMS (M+H⁺) m/z 202.1.

To a solution of (S)-tert-butyl 1-hydroxypent-4-en-2-ylcarbamate (165 g, 0.82 mol) and imidazole (72.5 g, 1.07 mol) in DCM (3 L) was added TBS-Cl (135.4 g, 0.9 mol). The reaction was stirred at RT overnight and filtered. The filtrate was concentrates. The resulting residue was dissolved in EtOAc (L) and washed with water and brine. The organic layer was dried over Na₂SO₄ and concentrated to give (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)pent-4-en-2-ylcarbamate (222.0 g), which was used in the next step without further purification. LRMS (M+H⁺) m/z 316.2.

To a solution of (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)pent-4-en-2-ylcarbamate (95 g, 0.3 mol) and MeI (46.7 mL, 0.75 mol) in DMF (500 mL) was added sodium hydride (60%, 18 g, 0.45 mol) at 0° C. The reaction was stirred at 0° C. for 3 h and LC-MS showed the reaction was complete. The reaction was quenched with saturated NH₄Cl solution and filtered. The filtrate was concentrated to remove most of DMF and the residue was dissolved in EtOAc (1.5 L). The organic layer was washed with water and brine, dried over Na₂SO₄. The above steps were repeated with another 127 g of (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)pent-4-en-2-ylcarbamate. The organic layers were combined and concentrated. The resulting residue was purified on silica gel column using a mixture of hexanes and EtOAc to give (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)pent-4-en-2-yl(methyl)carbamate (120 g, 40% for 4 steps). LRMS (M+H⁺) m/z 230.2.

To a solution of (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)pent-4-en-2-yl(methyl)carbamate (3.4 g, 10.3 mmol) in methanol (10 mL) was added HCl (4.0 M in 1,4-dioxane, 25 mL, 0.10 mol). The resulting solution was stirred for 2 h. The solvent was removed, and the remaining residue was dried under vacuum to give (S)-2-(methylamino)pent-4-en-1-ol as a HCl salt, which was used without further purification. LRMS (M+H⁺) m/z 116.2.

To a solution of 4-nitrophenylchloroformate 8 (2.28 g, 11.3 mmol) in THF (10 mL) was added a solution of 2-chloro-3-fluorobenzylamine hydrochloride (2.22 g, 11.3 mmol) and DIEA (5.38 mL, 30.9 mmol) in THF (10 mL). The resulting solution was stirred at RT for 20 min. The reaction solution was added into a solution of (S)-2-(methylamino)pent-4-en-1-ol hydrochloride (10.3 mmol), DIEA (5.38 mL, 30.9 mmol) in THF (100 mL). The resulting solution was stirred at RT for 1 h. The solvent was removed, and the resulting residue was purified on silica gel column using a mixture of DCM and MeOH to give (S)-3-(2-chloro-3-fluorobenzyl)-1-(1-hydroxypent-4-en-2-yl)-1-methylurea (2.56 g, 82%) as a white solid. LRMS (M+H⁺) m/z 301.2.

To a solution of (S)-3-(2-chloro-3-fluorobenzyl)-1-(1-hydroxypent-4-en-2-yl)-1-methylurea (2.0 g, 6.65 mmol) and toluene (50 mL) was added 6-fluoro-isoquinoline-3-carbonyl azide (1.58 g, 7.32 mmol). The resulting solution was stirred at 100° C. for 1 h. The solvent was removed, and the remaining residue was purified on silica gel column using a mixture of DCM and MeOH to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pent-4-enyl 6-fluoroisoquinolin-3-ylcarbamate (2.50 g, 77%). LRMS (M+H⁺) m/z 489.1.

To a solution of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pent-4-enyl 6-fluoroisoquinolin-3-ylcarbamate (0.9 g, 1.84 mmol) in THF (24 mL) and water (6 mL) were added 4-methylmorpholine N-oxide (1.08 g, 9.2 mmol), osmium tetroxide (46.8 mg, 0.184 mmol) and pyridine (15 uL, 0.184 mmol). The resulting solution was stirred for 1 h. The reaction was monitored with LC/MS and additional osmium tetroxide (46.8 mg, 0.184 mmol) was added. The resulting solution was stirred for 1 h. Sodium sulfite (5 g) and sodium bicarbonate (5 g) were added into the reaction. The resulting mixture was stirred for 1 h. The solid was then removed by filtration. The filtrate was diluted with ethyl acetate (100 mL) and washed with saturated sodium bicarbonate. The organic layer was concentrated, and the resulting residue was purified on silica gel column using a mixture of DCM and MeOH to give (2S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl 6-fluoroisoquinolin-3-ylcarbamate (0.9 g, 93%). LRMS (M+H⁺) m/z 523.2.

Example 10 Preparation of (2S)-2-((2-chloro-3-fluorobenzyl)(methyl)amino)-4-hydroxy-5-(phosphonooxy)pentyl 6-fluoroisoquinolin-3-ylcarbamate

To a solution of (2S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl 6-fluoroisoquinolin-3-ylcarbamate (0.25 g, 0.478 mmol, 1.0 equiv.), DIEA (0.416 mL, 2.39 mmol, 5 equiv.) and DMAP (0.117 g, 0.956 mmol, 2.0 equiv.) in anhydrous DCM (10 mL) was added dimethyl chlorophorophosphate (0.103 mL, 0.956 mmol, 2.0 equiv.) at RT. After the reaction mixture was stirred at RT for 30 min, an additional portion of dimethyl chlorophorophosphate (0.103 mL, 0.956 mmol, 2.0 equiv.) and DIEA (0.167 mL, 0.956 mmol, 2 equiv.) were added. The reaction was quenched with MeOH (5 mL). The solvent was removed and the resulting residue was dissolved in EtOAc (100 mL). The organic layer was washed with saturated NaHCO₃, water and brine, concentrated, and the resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (2S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(dimethoxyphosphoryloxy)-4-hydroxypentyl 6-fluoroisoquinolin-3-ylcarbamate (150 mg, 50%). LRMS (M+H⁺) m/z 631.2.

To a solution of (2S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(dimethoxyphosphoryloxy)-4-hydroxypentyl 6-fluoroisoquinolin-3-ylcarbamate (0.15 g, 0.238 mmol, 1.0 equiv.) in acetonitrile (2 mL) was added TMSI (0.162 mL, 1.19 mmol, 5.0 equiv.) at RT After stirred at RT for 10 min, the reaction was quenched with MeOH. The solvent was removed, and the resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O (0.1% TFA buffer) to give the desired product. The product was dissolved in a mixture of methanol and water (2:1), and HCl (4 M in 1,4-dioxane, 2 mL) was added. The solvent was removed. This procedure was repeated to give (2S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4-hydroxy-5-(phosphonooxy)pentyl 6-fluoroisoquinolin-3-ylcarbamate (98 mg, 64%) as a HCl salt. LRMS (M+H⁺) m/z 603.0.

Example 11 Preparation of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-oxo-5-(piperazin-1-yl)pentyl 6-fluoroisoquinolin-3-ylcarbamate

To a solution of (S)-methyl 4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-hydroxypentanoate (1.06 g, 3.06 mmol, 1.0 equiv) in toluene (12 mL) were added 6-fluoro-isoquinoline-3-carbonyl azide (661 mg, 3.06 mmol, 1.0 equiv). The reaction mixture was heated under 100° C. for 1 h and purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (S)-methyl 4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(6-fluoroisoquinolin-3-ylcarbamoyloxy)pentanoate (400 mg). LRMS (M+H⁺) m/z 535.2.

To a solution of (S)-methyl 4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(6-fluoroisoquinolin-3-ylcarbamoyloxy)pentanoate (400 mg, 0.748 mmol, 1.0 equiv.) in 1,4-dioxane (1 mL) was added LiOH (2 N, 1.5 mL, 2.99 mmol, 4.0 equiv.). The reaction mixture was stirred at RT for 1 h., then was acidified to pH 1-3 with HCl (1 N). The mixture was diluted in EtOAc. The organic layer was washed by H₂O and brine, and concentrated. The resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (S)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(6-fluoroisoquinolin-3-ylcarbamoyloxy)pentanoic acid (340 mg, 87%). LRMS (M+H⁺) m/z 521.2.

To a solution of (S)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(6-fluoroisoquinolin-3-ylcarbamoyloxy)pentanoic acid (83 mg, 0.160 mmol, 1.0 equiv) in DMF (1 mL) were added HBTU (72 mg, 0.191 mmol, 1.2 equiv.), tert-butyl-1-piperazine carboxylate (59 mg, 0.320 mmol, 2.0 equiv.) and DIEA (83 μL, 0.480 mmol, 3.0 equiv.). The reaction mixture was stirred 1 h at RT and purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (S)-tert-butyl 4-(4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(6-fluoroisoquinolin-3-ylcarbamoyloxy)pentanoyl)piperazine-1-carboxylate (61 mg, 55%). LRMS (M+H⁺) m/z 689.3.

To a solution of (S)-tert-butyl 4-(4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(6-fluoroisoquinolin-3-ylcarbamoyloxy)pentanoyl)piperazine-1-carboxylate (56 mg, 0.081 mmol, 1.0 equiv.) in MeOH (1 mL) was added HCl (4 M in 1,4-dioxane, 1 mL). The mixture was stirred overnight and concentrated. The resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O. The fractions containing the product were combined and concentrated. The resulting solid was dissolved in EtOAc. The organic solution was washed with saturated NaHCO₃. HCl (4 N) was added into the organic solution. The solution was then concentrated to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-oxo-5-(piperazin-1-yl)pentyl 6-fluoroisoquinolin-3-ylcarbamate (35 mg, 65%) as a HCl salt. LRMS (M+H⁺) m/z 589.2.

Example 12 Preparation of (S)-2-(3-(2-chloro-4-fluorobenzyl)-1-methylureido)-6-hydroxyhexyl isoquinolin-3-ylcarbamate

To a solution of (S)-2-amino-6-methoxy-6-oxohexanoic acid (20 g, 95 mmol) in H₂O (50 mL) and 1,4-dioxane (150 mL) was added a solution of NaHCO₃ (20 g, 238 mmol, 2.5 equiv.) in H₂O (50 mL) dropwise at 0° C. Boc₂O (25 g, 114 mmol, 1.2 equiv.) was added in 3 portions. The mixture was warmed up to RT and stirred for 1 h. The organic solvent was removed. The aqueous solution was washed with ether (200 mL). The solution was cooled down to 0° C., adjusted to pH 3-4 with HCl (1 N). The solution was extracted with EtOAc (300 mL×2). The organic layers were combined, dried over MgSO₄, and concentrated to give (S)-2-(tert-butoxycarbonylamino)-6-methoxy-6-oxohexanoic acid (23.5 g, 90%). LRMS (M-Boc+H⁺) m/z 176.1.

To a solution of (S)-2-(tert-butoxycarbonylamino)-6-methoxy-6-oxohexanoic acid (23.5 g, 85 mmol) in anhydrous THF (100 mL) was added Et₃N (14.2 mL, 102 mmol, 1.2 equiv.). The solution was cooled down to 0° C. and isobutyl chloroformate (12.2 mL, 93.5 mmol, 1.1 equiv.) was added dropwise. The solution was stirred for 30 min. The precipitate was filtered off. The filtrate was cooled down to 0° C. and a suspension of sodium borohydride (6.5 g, 170 mmol, 2 equiv.) in H₂O (3 mL) was added in one portion. The reaction was stirred for 1 h, and quenched with saturated NH₄Cl. THF was removed. The residue was dissolved into EtOAc (400 mL) and extracted with saturated NH₄Cl twice. The organic layers were combined, dried and concentrated. The residue was purified on silica gel column (hexanes/EtOAc 1:1) to give (S)-methyl 5-(tert-butoxycarbonylamino)-6-hydroxyhexanoate (20 g, 90%) as a colorless oil. LRMS (M-Boc+H⁺) m/z 162.1.

To a solution of (S)-methyl 5-(tert-butoxycarbonylamino)-6-hydroxyhexanoate (12 g, 46 mmol) in DMF (100 mL) was added imidazole (7.8 g, 115 mmol, 2.5 equiv.). TBS-Cl (8.25 g, 55 mmol, 1.2 equiv.) was then added in 3 portions. The reaction was complete in 30 min. Diethyl ether (200 mL) and brine (300 mL) were added to the reaction solution. The organic layer was further washed with brine (300 mL), dried, and concentrated to give (S)-methyl 5-(tert-butoxycarbonylamino)-6-(tert-butyldimethylsilyloxy)hexanoate (15.9 g, 92%) as a colorless oil. LRMS (M-Boc+H⁺) m/z 276.1.

To a solution of (S)-methyl 5-(tert-butoxycarbonylamino)-6-(tert-butyldimethylsilyloxy)hexanoate (15 g, 40 mmol) in DMF (100 mL) was added iodomethane (17 g, 120 mmol, 3 equiv.) at 0° C. NaH (60%, 2.4 g, 60 mmol, 1.5 equiv.) was added in 3 portions. The reaction was stirred at RT for 2 h. EtOAc (150 mL) and brine (200 mL) were added to the reaction mixture. The organic layer was washed with brine (200 mL), dried, and concentrated to give (S)-methyl 5-(tert-butoxycarbonyl(methyl)amino)-6-(tert-butyldimethylsilyloxy)hexanoate (15.5 g, quant.) as a colorless oil. LRMS (M-Boc+H⁺) m/z 290.1.

To a solution of (S)-methyl 5-(tert-butoxycarbonyl(methyl)amino)-6-(tert-butyldimethylsilyloxy)hexanoate (6.2 g, 16 mmol) in THF (50 mL) was slowly added TBAF (1 M in THF, 48 mL, 3 equiv.). The reaction was stirred at RT for 1 h. THF was removed. The residue was extracted with EtOAc (100 mL) and brine (100 mL) twice. The organic layers were combined and concentrated. The resulting residue was purified on silica gel column (hexanes/EtOAc 1:1) (S)-methyl 5-(tert-butoxycarbonyl(methyl)amino)-6-hydroxyhexanoate (4.4 g, quant.) as a colorless oil. LRMS (M-Boc+H⁺) m/z 176.2.

To a solution of (S)-methyl 5-(tert-butoxycarbonyl(methyl)amino)-6-hydroxyhexanoate (4.4 g, 16 mmol) in DCM (50 mL) was added CDI (3.1 g, 19 mmol). The reaction was complete in 30 min. DCM was removed. The residue was purified on silica gel column (hexanes/EtOAc 1:1) to give (S)-2-(tert-butoxycarbonyl(methyl)amino)-6-methoxy-6-oxohexyl 1H-imidazole-1-carboxylate (5.1 g, 85%) as a colorless oil. LRMS (M+Na⁺) m/z 392.1

To a solution of (S)-2-(tert-butoxycarbonyl(methyl)amino)-6-methoxy-6-oxohexyl 1H-imidazole-1-carboxylate (2 g, 5.4 mmol) in DCM (10 mL) was added a solution of triethyloxonium hexafluorophosphate (1.61 g, 6.5 mmol, 1.2 equiv.) in DCM (5 mL) dropwise at 0° C. The solution was warmed up to RT and stirred for 15 min. A solution of isoquinolin-3-amine (0.94 g, 6.5 mmol, 1.2 equiv.) in DCM (5 mL) was added. The solution was stirred for overnight. DCM was removed and the residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (S)-methyl 5-(tert-butoxycarbonyl(methyl)amino)-6-(isoquinolin-3-ylcarbamoyloxy)hexanoate (1.4 g, 58%). LRMS (M+H⁺) m/z 446.2.

To s solution of (S)-methyl 5-(tert-butoxycarbonyl(methyl)amino)-6-(isoquinolin-3-ylcarbamoyloxy)hexanoate (2.0 g, 4.5 mmol) in MeOH (10 mL) at 0° C. was added HCl (4 M in 1,4-dioxane, 10 mL) dropwise. The solution was stirred at RT for 2 h. The solvents were removed under high vacuum to give (S)-methyl 6-(isoquinolin-3-ylcarbamoyloxy)-5-(methylamino)hexanoate (1.8 g, 94%) as a yellow solid. LRMS (M+H⁺) m/z 346.2.

To a solution of triphosgene (71 mg, 0.24 mmol, 0.4 equiv.) in THF (5 mL) were added a solution of 2-chloro-4-fluorobenzylamine (95 mg, 0.6 mmol) and DIEA (0.22 mL, 1.26 mmol, 2.2 equiv.) in THF (5 mL) dropwise at 0° C. under N₂. The mixture was stirred at 0° C. for 30 min. A solution of (S)-methyl 6-(isoquinolin-3-ylcarbamoyloxy)-5-(methylamino)hexanoate (0.23, 0.6 mmol) and DIEA (0.11 mL, 0.66 mmol, 1.1 equiv.) in THF (5 mL) was added. The mixture was stirred at RT for 1 h. THF was removed. The residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (S)-methyl 5-(3-(2-chloro-4-fluorobenzyl)-1-methylureido)-6-(isoquinolin-3-ylcarbamoyloxy)hexanoate (0.18 g, 56%) as a white solid. LRMS (M+H⁺) m/z 531.2.

To a solution of (S)-methyl 5-(3-(2-chloro-4-fluorobenzyl)-1-methylureido)-6-(isoquinolin-3-ylcarbamoyloxy)hexanoate (80 mg, 0.15 mmol) in MeOH (1 mL) and THF (1 mL) was added LiBH₄ (2 M in THF, 0.3 mL, 4 equiv.) dropwise. The reaction was stirred at RT for 2 h. The reaction was quenched with saturated NH₄Cl (5 mL). The mixture was extracted with EtOAc (10 mL). The organic layer was concentrated. The resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (S)-2-(3-(2-chloro-4-fluorobenzyl)-1-methylureido)-6-hydroxyhexyl isoquinolin-3-ylcarbamate as a white solid 10 (40 mg, 53%). LRMS (M+H⁺) m/z 503.5.

Example 13 Preparation of (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-6-(phosphonooxy)hexyl isoquinolin-3-ylcarbamate

To a solution of (S)-methyl 5-(3-(2,3-difluorobenzyl)-1-methylureido)-6-(isoquinolin-3-ylcarbamoyloxy)hexanoate (1.45 g, 2.04 mmol, 1.0 equiv.) in 1,4-dioxane (18 mL) was added aqueous LiOH (6.12 mL, 6.12 mmol, 3.0 equiv.) at RT After stirred at RT for 1 h, the reaction mixture was acidified with HCl (1.0 N) to pH ˜3. The mixture was extracted with EtOAc twice. The combined EtOAc solution was washed with brine, dried over Na₂SO₄, and concentrated under vacuum to give (S)-5-(3-(2,3-difluorobenzyl)-1-methylureido)-6-(isoquinolin-3-ylcarbamoyloxy)hexanoic acid, which was used without further purification. LRMS (M+H⁺) m/z 501.3.

To a solution of (S)-5-(3-(2,3-difluorobenzyl)-1-methylureido)-6-(isoquinolin-3-ylcarbamoyloxy)hexanoic acid (˜2.04 mmol, 1.0 equiv.) and triethylamine (0.38 mL, 2.78 mmol, 1.2 equiv.) in anhydrous THF (7 mL) was added isopropyl chloroformate (2.80 mL, 2.80 mmol, 1.2 equiv.) dropwise at 0° C. After stirred at RT for 20 min, the mixture was filtered and transferred to a solution of NaBH₄ (0.18 g, 4.76 mmol, 2.0 equiv.) in water (2.0 mL). The resulting mixture was stirred at RT for 1 h, and quenched with saturated NH₄Cl. The solution was extracted with EtOAC twice. The organic layers were washed with brine, dried over Na₂SO₄, and concentrated. The resulting residue was purified on silica gel column (50-100% EtOAc in hexanes followed by 10% MeOH in dichloromethane) to give (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-6-hydroxyhexyl isoquinolin-3-ylcarbamate (0.58 g, 52% for two steps). LRMS (M+H⁺) m/z 487.3.

To a solution of (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-6-hydroxyhexyl isoquinolin-3-ylcarbamate (0.25 g, 0.51 mmol, 1.0 equiv.), DIEA (0.45 mL, 2.57 mmol, 5 equiv.) and DMAP (0.12 g, 1.53 mmol, 3.0 equiv.) in anhydrous dichloromethane (2.0 mL) was added dimethylphosphoryl chloride (0.18 mL, 1.53 mmol, 3.0 equiv.) at RT After stirred at RT for 45 min, the reaction mixture was extracted with EtOAc. The organic layer was washed with saturated NaHCO₃, water and brine, dried over Na₂SO₄, and concentrated to give (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-6-(dimethoxyphosphoryloxy)hexyl isoquinolin-3-ylcarbamate (0.28 g, 93%), which was used without further purification. LRMS (M+H⁺) m/z 595.3.

To a solution of (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-6-(dimethoxyphosphoryloxy)hexyl isoquinolin-3-ylcarbamate (0.28 g, 0.47 mmol, 1.0 equiv.) in acetonitrile (25 mL) was added TMSI (0.28 mL, 1.88 mmol, 4.0 equiv.) at RT After stirred at RT for 15 min, the reaction was quenched with MeOH. The solvent was concentrated. The resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O with 0.1% TFA. The fractions containing the product were combined and concentrated. The resulting residue was suspended in EtOAc, 5 drops of HCl (4 M in 1,4-dioxane) were added, and the organic solvent was removed. This procedure was repeated to give (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-6-(phosphonooxy)hexyl isoquinolin-3-ylcarbamate (0.16 g, 57%) as a HCl salt. LRMS (M+H⁺) m/z 567.2.

Example 14 Preparation of (S)-3-(2-aminoacetamido)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)propyl 6-fluoroisoquinolin-3-ylcarbamate

To a solution of (S)-tert-butyl 1-(benzyloxy)-3-hydroxypropan-2-ylcarbamate (1.89 g, 6.4 mmol) in DCM (50 mL) was added MSCl (0.55 mL, 7.04 mmol) and DIEA (1.27 mL, 7.68 mmol). The mixture was stirred at RT for 30 min. The mixture was diluted with DCM (300 mL), washed with NaHCO₃ and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The crude product was dissolved in DMF (20 mL). To this DMF solution was added NaN₃ (1.25 g, 19.2 mmol) and the mixture was heated to 80° C. for 6 h. LCMS indicated the completion of the reaction. The mixture was cooled to RT, water (20 mL) and EtOAc (200 mL) were added. The organic layer was separated, washed with NaHCO₃, brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The rude was purified on silica gel column to give (S)-tert-butyl 1-azido-3-(benzyloxy)propan-2-ylcarbamate (1.5 g, 73% for 2 steps).

To a solution NaH (0.29 g, 7.35 mmol) in DMF (10 mL) was added a solution of (S)-tert-butyl 1-azido-3-(benzyloxy)propan-2-ylcarbamate (1.5 g, 4.9 mmol) in DMF (10.0 mL). The mixture was stirred for 30 min. MeI (1.0 mL, 9.8 mmol) was then added. The mixture was stirred for another 2 h. LCMS indicated the completion of the reaction. The mixture was quenched with saturated NH₄Cl solution and extracted with EtOAc (200 mL×2). The organic layers were combined, washed with brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure to give (S)-tert-butyl 1-azido-3-(benzyloxy)propan-2-yl(methyl)carbamate (1.8 g), which was used without purification.

To a solution of (S)-tert-butyl 1-azido-3-(benzyloxy)propan-2-yl(methyl)carbamate (1.8 g of crude, 4.90 mmol) in MeOH (20 mL) was added Pd/C (300 mg). The mixture was transferred to an autoclave reactor, charged with 45 psi of hydrogen, and stirred overnight. The solid was filtered off and the filtrate was added CbzCl (0.83 mL, 5.88 mmol) and DIEA (1.22 mL, 7.35 mmol) and stirred for 30 min. LCMS indicated the completion of the reaction. The reaction mixture was concentrated under reduced pressure, dissolved in EtOAc, washed with NaHCO₃, brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure to give (S)-tert-butyl 1-(benzyloxycarbonylamino)-3-hydroxypropan-2-yl(methyl)carbamate (2.2 g), which was used without purification. LRMS (M+H⁺-Boc) m/z 239.1.

To a solution of (S)-tert-butyl 1-(benzyloxycarbonylamino)-3-hydroxypropan-2-yl(methyl)carbamate (2.2 g, ˜4.90 mmol) in toluene (20 mL) was added 6-fluoro-isoquinoline-3-carbonyl azide (1.16 g, 5.39 mmol) in portions and the mixture was heated to 100° C. for 1 h. The mixture was concentrated to one forth of the amount and purified on silica gel column to give (S)-3-benzyloxycarbonylamino-2-((1-tert-butoxycarbonyl)(methyl)amino)propyl 6-fluoroisoquinolin-3-ylcarbamate (1.5 g, 58% for 4 steps). LRMS (M+H⁺) m/z 527.3.

To a solution of (S)-3-benzyloxycarbonylamino-2-((1-tert-butoxycarbonyl)(methyl)amino)propyl 6-fluoroisoquinolin-3-ylcarbamate (1.5 g, 2.85 mmol) in DCM (10.0 mL) was added TFA (1.0 mL). The mixture was stirred for 1 h, concentrated, and re-dissolved in THF (5 mL). To this THF solution was added pre-stirred solution of 4-nitrophenylchloroformate and 2-chloro-3-fluorobenzylamine in THF (15 mL). The reaction mixture was stirred overnight. The mixture was concentrated under reduced pressure, re-dissolved in MeOH, filtered, and purified by RP-HPLC using a mixture of acetonitrile and H₂O to give (S)-3-benzyloxycarbonylamino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)propyl 6-fluoroisoquinolin-3-ylcarbamate (1.3 g, 75%). LRMS (M+H⁺) m/z 612.2.

To a solution of (S)-3-benzyloxycarbonylamino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)propyl 6-fluoroisoquinolin-3-ylcarbamate (1.3 g, 2.13 mmol) in CH₃CN (20.0 mL) was added TMSI (0.35 mL, 2.56 mmol). The mixture was stirred for 15 min. MeOH (20.0 mL) was added and stirring continued another 15 min. The mixture was concentrated and partitioned between diethyl ether (30 mL) and HCl (2 N, 20 mL). The aqueous layer was separated, adjusted to pH 9, extracted with EtOAc (200 mL×2). The combined organic layers were washed brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure to give an crude oil, which was dissolved in DMF (6.0 mL). To this DMF solution were added Boc-Gly-OH (0.36 g, 2.03 mmol) and HBTU (0.77 g, 2.03 mmol). The mixture was stirred for 1 h. The crude was filtered and purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (S)-3-(2-tert-butoxycarbonylaminoacetamido)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)propyl 6-fluoroisoquinolin-3-ylcarbamate (0.91 g, 78%). LRMS (M+H⁺) m/z 635.2.

To a solution of (S)-3-(2-tert-butoxycarbonylaminoacetamido)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)propyl 6-fluoroisoquinolin-3-ylcarbamate (0.87 g, 1.37 mmol) in DCM (30.0 mL) was added TFA (3.0 mL). The mixture was stirred for 1 h. The mixture was concentrated and dissolved in EtOAc. The EtOAc solution was washed with Na₂CO₃, brine, dried over Na₂SO₄, and filtered. To the filtrate was added HCl (4 M in dioxane, 0.7 mL, 2.8 mmol,). The organic solvent was removed under reduced pressure to give (S)-3-(2-aminoacetamido)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)propyl 6-fluoroisoquinolin-3-ylcarbamate (730 mg, 93%) as a HCl salt. LRMS (M+H⁺) m/z 535.2.

Example 15 Preparation of (S)-5-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentyl 5-(trifluoromethyl)pyridin-2-ylcarbamate

A mixture of (S)-5-amino-2-(benzyloxycarbonylamino)pentanoic acid (10.0 g, 37.56 mmol), ethyl 1,3-dioxoisoindoline-2-carboxylate (9.04 g, 41.28 mmol) in NMP (40.0 mL) was heated to 150° C. for 30 min in 4 microwave reaction tubes. The mixture was diluted with EtOAc (500 mL). The organic layer washed with water (100 mL×2), brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure to give an oil, which was dissolved in toluene. To this toluene solution was added paraformaldehyde, PTSA and molecular sieves (3 Å) and the mixture was heated to 150° C. for 20 min. The mixture was diluted with ether (800 mL), washed with NaHCO₃, brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The crude was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-benzyl 4-(3-(1,3-dioxoisoindolin-2-yl)propyl)-5-oxooxazolidine-3-carboxylate (11.6 g, 76% for 2 steps).

To a solution of (S)-benzyl 4-(3-(1,3-dioxoisoindolin-2-yl)propyl)-5-oxooxazolidine-3-carboxylate (11.6 g, 28.40 mmol) in DCM (30.0 mL) was added Et₃SiH (13.6 mL, 85.3 mmol). The reaction mixture was stirred overnight. The mixture was concentrated under reduced pressure and dissolved in THF (100 mL). To this THY solution was added tert-butyl chloroformate (4.4 mL, 34.08 mmol) at 0° C. followed by TEA (12.0 mL, 85.2 mmol) and stirred at RT for 30 min. The precipitate was filtered off and the filtrate was added into a NaBH₄ suspension in water (1.0 mL) at 0° C., and the mixture was stirred at RT for 30 min. LC/MS indicated the completion of the reaction. The mixture was acidified to pH 3 using HCl (1 N). The aqueous layer was extracted with EtOAc (300 mL×2). The combined organic layer was washed with NaHCO₃, brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The crude was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-benzyl 5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl(methyl)carbamate (5.01 g, 45%). LRMS (M+H⁺) m/z 397.3.

To a solution of (S)-benzyl 5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl(methyl)carbamate (5.01 g, 12.65 mmol) in MeOH (100 mL) was added Pd/C (1.0 g). The mixture was transferred to an autoclave reactor, charged with 50 psi of hydrogen, and stirred overnight. The mixture was filtered, and the filtrate was concentrated under reduced pressure to give (S)-2-(5-hydroxy-4-(methylamino)pentyl)isoindoline-1,3-dione (3.2 g, 97%). LRMS (M+H⁺) m/z 263.1

To a solution of 4-nitrophenylchloroformate (460 mg, 2.29 mmol) in THF (20 mL) was added 2-chloro-3-fluorobenzylamine hydrochloride (626 mg, 2.29 mmol) and DIEA (0.76 mL, 4.58 mmol) and the mixture was stirred at RT until TLC showed complete consumption of 2-chloro-3-fluorobenzylamine. The mixture was then added into a solution of (S)-2-(5-hydroxy-4-(methylamino)pentyl)isoindoline-1,3-dione (500 mg, 1.91 mmol) in THF (10 mL). The mixture was stirred overnight, concentrated and purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (S)-3-(2-chloro-3-fluorobenzyl)-1-(5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl)-1-methylurea (401 mg, 47%). LRMS (M+H⁺) m/z 448.3.

To a solution of (S)-3-(2-chloro-3-fluorobenzyl)-1-(5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl)-1-methylurea (200 mg, 0.45 mmol), 5-(trifluoromethyl)picolinic acid (256 mg, 1.35 mmol) and DMA (0.3 mL, 1.35 mmol) in toluene (5 mL) was added DPPA (0.27 mL, 1.35 mmol). The mixture was heated to 100° C. for 2 h, and concentrated. The resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(1,3-dioxoisoindolin-2-yl)pentyl 5-(trifluoromethyl)pyridin-2-ylcarbamate (150 mg, 80%). LRMS (M+Na⁺) m/z 658.2.

To a solution of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(1,3-dioxoisoindolin-2-yl)pentyl 5-(trifluoromethyl)pyridin-2-ylcarbamate (150 mg, 0.24 mmol) in MeOH (5.0 mL) was added NH₂NH₂ (0.2 mL). The reaction mixture was stirred at RT for 2 h. The mixture was concentrated, dissolved in MeOH, filtered, and purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (S)-5-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentyl 5-(trifluoromethyl)pyridin-2-ylcarbamate (91 mg, 76%). LRMS (M+H⁺) m/z 506.1.

Example 16 Preparation of (S)-5-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentyl 2,7-naphthyridin-3-ylcarbamate

Ethyl 1-chloro-2,7-naphthyridine-3-carboxylate was prepared from 3-cyano-4-picoline according to the published procedures (E. Barbu et. al. Heterocyclic Communications, Vol. 6, No. 1, 2000, 25-28) with some modifications.

A mixture of 1-chloro-2,7-naphthyridine-3-carboxylate (320 mg, 1.352 mmol), ammonium formate (128 mg, 2.0 mmol), 10% Pd/C (33 mg), EtOAc (5 mL) and MeOH (5 mL) was refluxed for 10 min. The mixture was filtered and concentrated. The resulting residue was purified by RP-HPLC using a mixture of acetonitrile and H₂O to give 2,7-naphthyridine-3-carboxylate (265 mg, 72%). LRMS (M+H⁺) m/z 203.0.

A mixture of 2,7-naphthyridine-3-carboxylate (260 mg, 1.29 mmol), hydrazine (0.20 mL, 6.44 mmol) and ethanol was refluxed for 2 h and concentrated to dryness. The resulting residue was mixed with 2N HCl (1.3 mL, 2.60 mmol) and H₂O (5 mL) and cooled with an ice bath. To the mixture was added a solution of NaNO₂ (178 mg, 2.6 mmol in 1 mL H₂O) dropwise, the mixture was stirred at 0° C. for 1 h. The mixture was then neutralized with saturated NaHCO₃ and extracted with DCM. The DCM solution was washed with water, brine, dried and concentrated to give 2,7-naphthyridine-3-carbonyl azide as a pale yellow solid (244 mg, 95%). LRMS (M−N₂+H⁺) m/z 172.1.

A mixture of 2,7-naphthyridine-3-carbonyl azide (14 mg, 0.07 mmol), (S)-3-(2-chloro-3-fluorobenzyl)-1-(5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl)-1-methylurea (33 mg, 0.07 mmol) and toluene (2 mL) was stirred at 100° C. for 1 h and concentrated. The resulting residue was treated with hydrazine (0.2 mL) and methanol (1 mL) at RT for 1 h. Concentration followed by purification on RP-HPLC using a mixture of acetonitrile, H₂O and 0.1% TFA gave (S)-5-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentyl 2,7-naphthyridin-3-ylcarbamate as a TFA salt (28 mg, 53%). LRMS (M+H⁺) m/z 489.1.

Example 17 Preparation of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-oxo-5-(piperazin-1-yl)pentyl benzo[d]thiazol-2-ylcarbamate

A solution of (S)-methyl 4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-hydroxypentanoate (4.34 mmol) in toluene (43 mL) under nitrogen was heated to 100° C. in an oil bath. A slurry of benzo[d]thiazole-2-carbonyl azide (973 mg, 1.0 equiv.) in toluene (15 mL) was added in portions over 30 min. The reaction was maintained at 100° C. for 30 min. The solvent was removed in vacuo and the residue subjected to flash chromatography using a mixture of hexanes and EtOAc to give (S)-methyl 5-(benzo[d]thiazol-2-ylcarbamoyloxy)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentanoate as a yellow solid (2.35 g, quant.). LRMS (M+H⁺)=523.5.

To a solution of (S)-methyl 5-(benzo[d]thiazol-2-ylcarbamoyloxy)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentanoate (2.3 g, 4.4 mmol) in 1,4-dioxane (15 mL) was added LiOH (2 N, 4.4 mL, 2 equiv.). The reaction mixture was stirred at RT for 2 h. The mixture was acidified to pH ˜3 with HCl (1 N, ˜10 mL), and ethyl acetate (50 mL) was added. The organic layer was extracted with EtOAc (3×20 mL), dried over Na₂SO₄ and concentrated. A small sample (30 mg) was purified by RP-HPLC (20-100% ACN in H₂O) to give (S)-5-(benzo[d]thiazol-2-ylcarbamoyloxy)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentanoic acid as a white solid (8 mg). The remainder was used without further purification. LRMS (M−H⁺)=507.4.

To a solution of (S)-5-(benzo[d]thiazol-2-ylcarbamoyloxy)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentanoic acid (˜4.41 mmol) in DMF (8 mL) at RT were added N-Boc-piperazine (820 mg, 1 equiv.), DIEA (1.2 mL, 1.5 equiv.), and HBTU (2.00 g, 1.2 equiv.) The reaction was allowed to stir overnight, and the crude was purified by RP-HPLC (5-100% ACN in H₂O) to give (S)-tert-butyl 4-(5-(benzo[d]thiazol-2-ylcarbamoyloxy)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentanoyl)piperazine-1-carboxylate as a white solid (801 mg, 27% over 2 steps). LRMS (M+Na⁺)=699.4.

To a solution of (S)-tert-butyl 4-(5-(benzo[d]thiazol-2-ylcarbamoyloxy)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentanoyl)piperazine-1-carboxylate (713 mg, 1.05 mmol) in DCM (5 mL) was added TFA (1 mL) and allowed to stir for 30 min. The reaction mixture was concentrated, and the residue purified by RP-HPLC (20-100% ACN in H₂O) and concentrated to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-oxo-5-(piperazin-1-yl)pentyl benzo[d]thiazol-2-ylcarbamate as an off-white solid (430 mg, 71%). LRMS (M+H⁺)=577.1

Example 18 Preparation of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-oxo-5-(piperazin-1-yl)pentyl isoquinolin-3-ylcarbamate

To a solution of (S)-5-(hydroxymethyl)pyrrolidin-2-one (30.0 g, 261 mmol) and imidazole (23.1 g, 340 mmol) in DCM (900 mL) was added TBS-Cl (42.9 g, 288 mmol). The reaction mixture was stirred at RT for 30 min and filtered. The filtrate was washed with water and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-5-((tert-butyldimethylsilyloxy)methyl)pyrrolidin-2-one (50 g, 83.7%). LRMS (M+H⁺) m/z 230.2.

To a solution of (S)-5-((tert-butyldimethylsilyloxy)methyl)pyrrolidin-2-one (48.5 g, 0.21 mol) in THF (100 mL) was added t-BuOK (30.8 g, 0.27 mol) at 0° C. The mixture was stirred at 0° C. for 30 min followed by addition of Cbz-Cl (40.4 mL, 0.27 mol) dropwise at 0° C. The resulting mixture was stirred at RT overnight, quenched with saturated NH₄Cl, concentrated to a small amount, and diluted with EtOAc. The organic layer was washed with water and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-benzyl 2-((tert-butyldimethylsilyloxy)methyl)-5-oxopyrrolidine-1-carboxylate (70 g, 91%). LRMS (M+H−44) m/z 320.2.

To a solution of (S)-benzyl 2-((tert-butyldimethylsilyloxy)methyl)-5-oxopyrrolidine-1-carboxylate (39 g, 0.107 mol) in THF (214 mL) was added LiOH (2 N, 107.4 mL). The reaction mixture was stirred at RT overnight, concentrated to dryness, and dissolved in DMF (100 mL). To the resulting solution were added HBTU (48.9 g, 0.13 mmol) and Boc-piperazine (24 g, 0.13 mol). The reaction mixture was stirred at RT for 1 h and diluted with water (200 mL) and EtOAc (500 mL). The organic layer was washed with water, dried over Na₂SO₄, filtered and concentrated. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-tert-butyl 4-(4-(benzyloxycarbonylamino)-5-(tert-butyldimethylsilyloxy)pentanoyl)piperazine-1-carboxylate (33.3 g, 56.5%). LRMS (M+H) m/z 550.3.

To a solution of (S)-tert-butyl 4-(4-(benzyloxycarbonylamino)-5-(tert-butyldimethylsilyloxy)pentanoyl)piperazine-1-carboxylate (32.3 g, 58.8 mmol) and iodomethane (7.3 mL, 117.6 mmol) in DMF (450 mL) was added solid sodium hydride (60%, 3.5 g, 88.2 mmol) at 0-5° C. The mixture was stirred at 0-5° C. for 30 min and quenched with saturated NH₄Cl solution. The mixture was concentrated to remove most of DMF under high vacuum. The residue was dissolved in EtOAc (700 mL). The organic mixture was washed with water and brine, dried over Na₂SO₄, filtered, and concentrated to give (S)-tert-butyl 4-(4-((benzyloxycarbonyl)(methyl)amino)-5-(tert-butyldimethylsilyloxy)pentanoyl)piperazine-1-carboxylate (34 g, crude), which was used without further purification. LRMS (M+H) m/z 564.3.

(S)-tert-butyl 4-(4-((benzyloxycarbonyl)(methyl)amino)-5-(tert-butyldimethylsilyloxy)pentanoyl)piperazine-1-carboxylate (21.5 g) and 10% Pd/C (2.2 g) in ethanol (100 mL) was charged with H₂ (50 psi). The resulting mixture was stirred at RT overnight and filtered. The filtrate was concentrated to give (S)-tert-butyl 4-(5-(tert-butyldimethylsilyloxy)-4-(methylamino)pentanoyl)piperazine-1-carboxylate (16 g, crude), which was sued without further purification. LRMS (M+H) m/z 430.3.

To a solution of (S)-tert-butyl 4-(5-(tert-butyldimethylsilyloxy)-4-(methylamino)pentanoyl)piperazine-1-carboxylate (16 g, 37.3 mmol) and DIEA (1.3 mL, 7.46 mmol) in THF (180 mL) was added 4-nitrophenyl 2-chloro-3-fluorobenzylcarbamate (12 g, 37.3 mmol). The reaction mixture was stirred at RT for 2 h and concentrated. The residue was purified on silica gel using a mixture of EtOAc and hexanes to give (S)-tert-butyl 4-(5-(tert-butyldimethylsilyloxy)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentanoyl)piperazine-1-carboxylate (14.3 g, 62.4% for three steps). LRMS (M+H) m/z 615.3.

To a solution of (S)-tert-butyl 4-(5-(tert-butyldimethylsilyloxy)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentanoyl)piperazine-1-carboxylate (14 g, 22.8 mmol) in THF (70 mL) was added TBAF (1M, 34.2 mL, 34.2 mmol). The reaction mixture was stirred at RT for 1 h and concentrated. The residue was dissolved in EtOAc (500 mL). The organic mixture was washed with 2% citric acid, NaOH (0.2 N), and brine, dried over Na₂SO₄, filtered, and concentrated to give (S)-tert-butyl 4-(4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-hydroxypentanoyl)piperazine-1-carboxylate (12.1 g, crude), which was used without further purification. LRMS (M+H) m/z 501.2.

To a solution of (S)-tert-butyl 4-(4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-hydroxypentanoyl)piperazine-1-carboxylate (11.2 g, 22.4 mmol) in toluene (110 mL) was added isoquinoline-3-carbonyl azide (4.7 g, 23.5 mmol). The reaction mixture was stirred at 100° C. for 30 min and concentrated. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-tert-butyl 4-(4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(isoquinolin-3-ylcarbamoyloxy)pentanoyl)piperazine-1-carboxylate (10.8 g, 72%). LRMS (M+H) m/z 671.3.

To a solution of (S)-tert-butyl 4-(4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(isoquinolin-3-ylcarbamoyloxy)pentanoyl)piperazine-1-carboxylate (22 g, 32.8 mmol) in DCM (200 mL) was added TFA (100 mL). The reaction mixture was stirred at RT for 3 h and concentrated. The residue was purified on silica gel column using a mixture of MeOH and DCM. The fractions were concentrated, dissolved in water (200 mL), neutralized to pH 8-9 with 1N NaOH, and extracted with EtOAc (300 mL×3). The organic layer was dried over Na₂SO₄, filtered, and concentrated to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-oxo-5-(piperazin-1-yl)pentyl isoquinolin-3-ylcarbamate (14 g, 75%). LRMS (M+H) m/z 571.1.

Example 19 Preparation of (S)-2-((2-chloro-3-fluorobenzyl)(methyl)amino)-5-(4-isopropylpiperazin-1-yl)-5-oxopentyl isoquinolin-3-ylcarbamate

To a solution of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-oxo-5-(piperazin-1-yl)pentyl isoquinolin-3-ylcarbamate (610 mg, 1.07 mmol) in acetone (1 mL) and DCM (1 mL) was added acetic acid (4 drops, ˜0.2 mL). The reaction mixture was stirred at RT for 30 min. To this mixture was added solid NaBH(OAc)₃ and the resulting mixture was stirred at RT for 1 h and concentrated. The residue was purified on RP-HPLC using a mixture of acetonitrle and water (0.1% HCOOH buffer). The fractions was collected, concentrated to dryness, and re-dissolved in EtOAc. The organic mixture was washed with Na₂CO₃, dried over Na₂SO₄, filtered, and concentrated to give (S)-2-((2-chloro-3-fluorobenzyl)(methyl)amino)-5-(4-isopropylpiperazin-1-yl)-5-oxopentyl isoquinolin-3-ylcarbamate (540 mg, 82%) as white solid. LRMS (M+H⁺) m/z 613.3.

Example 20 Preparation of Isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-3-(2,3-dihydroxy-propoxy)-propyl ester

To a mixture of (R)-Solketal (1.85 g, 14.0 mmol), and 2,6-lutidine (2.47 mL, 14.7 mmol) in dichloromethane (45 mL) cooled to 0° C. was added triflic anhydride (4.14 g, 14.7 mmol). The resulting solution was stirred for 2 h at 0° C. then concentrated to give trifluoromethanesulfonic acid 2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester which was used without further purification.

To a solution of boc-D-serinol (1.33 g, 4.73 mmol) in THF was added sodium hydride (60%, 0.378 g, 9.46 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 0.5 h then trifluoromethanesulfonic acid 2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester was slowly added over 5 min at 0° C. Once addition was complete reaction was warmed to room temperature and allowed to stir for 2 h. After 2 h, the reaction mixture was cooled to 0° C. and 4 mL of H₂O were added. Reaction mixture was then concentrated and the resulting residue was dissolved in EtOAc (200 mL). The organic layer was then washed with 1 M KHSO₄, saturated aq. NaHCO₃, brine, and dried over Na₂SO₄. Concentration of the organic layer afforded a yellow oil which was purified on silica gel column using a mixture of hexanes and EtOAc to give [2-benzyloxy-1-(2,2-dimethyl-[1,3]dioxolan-4-ylmethoxymethyl)-ethyl]-carbamic acid tert-butyl ester as a colorless oil (1.39 g, 72%). LRMS (M-Boc+H⁺) m/z 296.1.

To a solution of [2-Benzyloxy-1-(2,2-dimethyl-[1,3]dioxolan-4-ylmethoxymethyl)-ethyl]-carbamic acid tert-butyl ester (1.26 g, 3.18 mmol) in DMF (10 mL) was added sodium hydride (60%, 0.19 g, 4.78 mmol) at 0° C. in one portion. The reaction was stirred at 0° C. for 0.5 h then MeI (1.36 g, 9.56 mmol) was added. The reaction mixture was then stirred at 0° C. for 3 h at which time the LC-MS showed the reaction was complete. The reaction was quenched with saturated aq. NH₄Cl solution and extracted with EtOAc (2×100 mL). The organic layer was then washed with water, brine and dried over Na₂SO₄. The organic layers were concentrated to give [2-benzyloxy-1-(2,2-dimethyl-[1,3]dioxolan-4-ylmethoxymethyl)-ethyl]-methyl-carbamic acid tert-butyl ester (1.25 g, 96%). LRMS (M-Boc+H⁺) m/z 310.1.

To a solution of crude [2-Benzyloxy-1-(2,2-dimethyl-[1,3]dioxolan-4-ylmethoxymethyl)-ethyl]-methyl-carbamic acid tert-butyl ester (1.25 g, 3.06 mmol) in MeOH (10 mL) was added Pd/C (300 mg). The mixture was transferred to an autoclave reactor, charged with 55 psi of hydrogen, and stirred. After 1.5 h, LCMS analysis indicated the completion of the reaction. The reaction mixture was then filtered through celite and concentrated under reduced pressure to give [1-(2,2-dimethyl-[1,3]dioxolan-4-ylmethoxymethyl)-2-hydroxy-ethyl]-methyl-carbamic acid tert-butyl ester (0.875 g, 95%), which was used without purification. LRMS (M-Boc+H⁺) m/z 220.2.

Isoquinoline-3-carbonyl azide (2.36 g, 11.9 mmol) was added to a solution of [1-(2,2-Dimethyl-[1,3]dioxolan-4-ylmethoxymethyl)-2-hydroxy-ethyl]methyl-carbamic acid tert-butyl ester (3.80 g, 11.9 mmol) in toluene (200 mL) were added isoquinoline-3-carbonyl azide (2.36 g, 11.9 mmol, 1.0 equiv). The reaction mixture was heated to 100° C. for 1 h and then concentrated. Purification on silica gel column using a mixture of hexanes and EtOAc to give isoquinolin-3-yl-carbamic acid 2-(tert-butoxycarbonyl-methyl-amino)-3-(2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-propyl ester (2.9 g, 50%). LRMS (M-Boc+H⁺) m/z 390.2.

To a solution of Isoquinolin-3-yl-carbamic acid 2-(tert-butoxycarbonyl-methyl-amino)-3-(2,2-dimethyl-[1,3]-dioxolan-4-ylmethoxy)-propyl ester (2.9 g, 5.93 mmol) in DCM (200 mL) was added TFA (12 mL) at 0° C. The mixture was stirred for 2 h, concentrated under reduced pressure, and re-dissolved in THF (10 mL) and DIEA (6.6 mL, 37.8 mmol). To this THF solution was added pre-stirred solution of 4-nitrophenylchloroformate (1.33 g, 6.62 mmol), 2-chloro-3-fluorobenzylamine (1.0 g, 6.3 mmol), and DIEA (1.2 mL, 6.9 mmol) in THF (85 mL) at 0° C. The reaction mixture was stirred for 2 h allowing the reaction to gradually warm to 24° C. The mixture was concentrated under reduced pressure, re-dissolved in MeOH, filtered, and purified by RP-HPLC using a mixture of acetonitrile and H₂O to give isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-3-(2,3-dihydroxy-propoxy)-propyl ester (1.1 g, 45% over two steps). LRMS (M+H⁺) m/z 535.1.

Example 21 Preparation of Isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-3-(2-hydroxy-3-phosphonooxy-propoxy)-propyl ester

To a mixture of isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-3-(2,3-dihydroxy-propoxy)-propyl ester (1.2 g, 2.25 mmol), DIEA (1.56 mL, 9.0 mmol) and DMAP (1.11 g, 9.0 mmol.) in anhydrous DCM (250 mL) was added diethyl chlorophorophosphate (1.3 mL, 9.0 mmol) at 0° C. After stirring the reaction at 0° C. for 10 min, LC/MS analysis revealed the reaction was complete. The reaction was quenched with MeOH (80 mL). The mixture was then concentrated and the resulting residue was dissolved in EtOAc (200 mL). The organic layer was washed with saturated aq. NaHCO₃, water, brine and concentrated. The resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-3-[3-(diethoxy-phosphoryloxy)-2-hydroxy-propoxy]-propyl ester (601 mg, 47%). LRMS (M+H⁺) m/z 671.2.

To a solution of Isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-3-[3-(diethoxy-phosphoryloxy)-2-hydroxy-propoxy]-propyl ester (0.60 g, 0.895 mmol) in acetonitrile (30 mL) was added TMSI (1.43 g, 7.16 mmol) dropwise at 0° C. After stirring at 0° C. for 4.5 h, the reaction was quenched with EtOH. The solvent was removed, and the resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O (0.1% TFA buffer) to give isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-3-(2-hydroxy-3-phosphonooxy-propoxy)-propyl ester (396 mg, 73%). LRMS [M−H]⁺ m/z 613.5

To a solution of Isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-3-(2-hydroxy-3-phosphonooxy-propoxy)-propyl ester (0.15 g, 0.238 mmol) in MeOH (50 mL) was added 0.1 M NaOH (12.8 mL, 1.28 mmol, at 0° C. (Note: pH was monitored closely making sure not to raise pH above 8). After stirring at 0° C. for 1 h, the solvent was removed and the resulting residue was dissolved in 4 mL of H₂O. The solution was then frozen in a dry-ice bath and placed under high vacuum until all the H₂O is removed to give isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-3-(2-hydroxy-3-phosphonooxy-propoxy)-propyl ester disodium salt (410 mg). LRMS (M−2Na+3H⁺) m/z 613.5.

Example 22 Preparation of Isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-5-(4-methyl-piperazin-1-yl)-pentyl ester

To a solution of 5-hydroxymethyl-pyrrolidin-2-one (20 g, 0.174 mol) in DMF (100 mL) was added imidazole (17.7 g, 0.260 mol) followed by TBDMSCl (27.5 g, 0.182 mol). After 2.5 h, LCMS analysis revealed reaction was complete. EtOAc (600 mL) and brine (300 mL) were added to the reaction solution. The aqueous layer was further extracted with EtOAc (2×350 mL). The combined organic layers were washed with brine, dried, and concentrated to give 5-(tert-butyl-dimethyl-silanyloxymethyl)-pyrrolidin-2-one (39.5 g) as a light yellow oil which was used in the next step without further purification. LRMS (M+H⁺) m/z 230.1.

To a solution of 5-(tert-butyl-dimethyl-silanyloxymethyl)-pyrrolidin-2-one (39.5 g of crude material, 173.7 mmol) in CH₃CN (570 mL) was added Boc₂O (41.7 g, 0.238 mol) and DMAP (2.11 g, 17.4 mmol). The mixture was stirred for 14 h at 24° C. The organic solvent was removed affording an oil which was purified on silica gel column using a mixture of hexanes and EtOAc to give 2-(tert-butyl-dimethyl-silanyloxymethyl)-5-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester (50.9 g, 89% over two steps). LRMS (M-Boc+H⁺) m/z 230.1.

To a solution of 2-(tert-butyl-dimethyl-silanyloxymethyl)-5-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester (50.2, 0.152 mmol in MeOH (500 mL) was added NaOMe (30% in MeOH, 12 mL) and stirred at 24° C. After 1 h, LCMS analysis indicated reaction was complete. The reaction mixture was then treated with saturated aq. NH₄Cl (15 mL) and concentrated. The resulting residue was purified on silica gel column using a mixture of hexanes and EtOAc to give 4-tert-butoxycarbonylamino-5-(tert-butyl-dimethyl-silanyloxy)-pentanoic acid methyl ester (46.8 g, 85%). LRMS (M-Boc+H⁺) m/z 262.2.

To a solution of (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)pent-4-en-2-ylcarbamate (20 g, 55.0 mmol) and MeI (6.22 mL, 99.7 mmol) in DMF (700 mL) was added sodium hydride (60%, 3.1 g, 77.6 mmol) at 0° C. The reaction was stirred at 0° C. for 2 h then warmed to 10° C. for an additional 2 h at which point LC-MS analysis showed the reaction was complete. The reaction was quenched with saturated aq. NH₄Cl solution (800 mL) and EtOAc (2 L). Water was then added to dissolve the solids. The organic layer was washed with water, brine, and dried over Na₂SO₄. The resulting residue was purified on silica gel column using a mixture of hexanes and EtOAc to give (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)pent-4-en-2-yl(methyl)carbamate (16.9 g, 81%). LRMS (M+H⁺) m/z 230.2.

To a solution of (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)pent-4-en-2-yl(methyl)carbamate (91.0 g, 242.6 mmol) in DCM (750 mL) was added TMSOTf (87.8 mL, 485.2 mmol) at 0° C. The mixture was stirred for 1 h, and then poured into saturated aq. NH₄Cl (1 L) and CH₂Cl₂ (1 L) (Note: water (700 mL) was added to dissolve salts). The organic layer was then washed with brine, dried over Na₂SO₄ and concentrated under reduced pressure. The resulting residue was re-dissolved in THF (300 mL) and DIEA (84.5 mL, 485.2 mmol). To this THF solution was added a pre-stirred solution of 4-nitrophenylchloroformate (56.3 g, 279.0 mmol), 2-chloro-3-fluorobenzylamine (46.5 g, 291.1 mmol), and DIEA (50.7 mL, 291.1 mmol) in THF (1.1 L) at 0° C. The reaction mixture was stirred for 2 h allowing the reaction to gradually warm to 24° C. at which point the LCMS analysis revealed reaction completion. The mixture was concentrated under reduced pressure and purified on silica gel column using a mixture of hexanes and EtOAc to give 5-(tert-butyl-dimethyl-silanyloxy)-4-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-pentanoic acid methyl ester (73.1 g, 65% over two steps). LRMS (M+H⁺) m/z 461.1.

To a solution of 5-(tert-Butyl-dimethyl-silanyloxy)-4-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-pentanoic acid methyl ester (21.0 g, 45.6 mmol) in THF (450 mL) was slowly added TBAF (1 M in THF, 68.4 mL, 68.4 mmol). The reaction was stirred at 24° C. for 1 h. THF was removed. The residue was diluted with EtOAc (600 mL) and washed with saturated aq. NH₄Cl and brine. The organic layers were dried over Na₂SO₄ and concentrated. The resulting residue was dissolved in toluene and added into a toluene solution of isoquinoline-3-carbonyl azide (9.07 g, 45.6 mmol) at 100° C. The reaction mixture was heated to 100° C. for 1 h and then concentrated. Resulting residue was purified on silica gel column using hexanes and EtOAc to give 4-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-5-(isoquinolin-3-ylcarbamoyloxy)-pentanoic acid methyl ester (16.8 g, 71%) as a colorless oil. LRMS (M+H⁺) m/z 517.1.

To a solution of 4-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-5-(isoquinolin-3-ylcarbamoyloxy)-pentanoic acid methyl ester (80 mg, 0.15 mmol) in THF (100 mL) was added DiBAL-H (1 M in heptanes, 12.2 mL, 12.2 mmol) dropwise at −78° C. The reaction was stirred at −78° C. for 2 h at which point another DiBAL-H aliquot (1 M in heptanes, 12.2 mL, 12.2 mmol) was added again. The reaction was stirred at −78° C. for 2 h and then NaBH₄ (0.33 g. 8.72 mmol) was added at −78° C. The reaction was stirred for an additional 2 h allowing the reaction to slowly warm to −20° C. then MeOH (20 mL) was added. The reaction mixture was then concentrated, re-dissolved in EtOAc, and washed with 0.5 N aq. HCl and brine. The organic layer was then dried over Na₂SO₄ and concentrated. The resulting residue was purified on silica gel column using CH₂Cl₂ and MeOH to give Isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-5-hydroxy-pentyl ester as a colorless oil (2.1 g, 74%). LRMS [M+H]⁺ m/z 489.1.

To a solution of Dess-Martin periodinane (2.40 g, 5.65 mmol) in anhydrous CH₂Cl₂ (100 mL) was added isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-5-hydroxy-pentyl ester (2.40 g, 4.92 mmol) at RT After 20 min at 24° C., the reaction was analyzed by LC/MS revealing reaction completion. The reaction was quenched with saturated aq. NaHCO₃ and 1N aq. Na₂S₂O₃ (40 mL each) and stirred for 0.5 h. The organic layer was separated washed brine, dried over Na₂SO₄ and then concentrated. The resulting residue was isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-5-oxo-pentyl ester which was used without further purification (2.37 g crude). LRMS (M+H⁺) m/z 487.1.

To a solution of isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-5-oxo-pentyl ester (2.37 g crude mixture, 4.92 mmol) in anhydrous DCE (5 mL) and AcOH 1 (1 mL) was added N-methyl piperazine (0.573 mL, 5.16 mmol) at RT After 3 h of stirring at RT, sodium triacetoxyborohydride (4.17 g, 19.7 mmol) was added in one portion followed by 10 mL DCE. The mixture was stirred for 2 h at RT, the diluted in CH₂Cl₂ and washed with aq. NaHCO₃ and brine. After drying the solution over Na₂SO₄, the reaction mixture was concentrated and the resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O with a TFA Buffer. The purified fractions were concentrated, redissolved in EtOAc and washed with saturated aq. NaHCO₃. Removal of the solvent afforded isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-5-(4-methyl-piperazin-1-yl)-pentyl ester as the free base (1.43 g, 51%) LRMS (M+H⁺) m/z 571.3.

Example 23 Preparation of Isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-5-(5,6-dihydro-8H-[1,2,4]triazolo[4,3-a]pyrazin-7-yl)-pentyl ester

To a solution of isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-5-oxo-pentyl ester (75 mg crude mixture, 0.15 mmol) in anhydrous DCE (2 mL) and DIEA (56 uL, 0.32 mmol) was added the triazolopiperazine HCl salt (27 mg, 0.17 mmol) at RT. After 5 min of stirring at RT, sodium triacetoxyborohydride (98 mg, 0.45 mmol) was added in one portion. The slurry was stirred for 16 h at RT, the diluted in CH₂Cl₂ and washed with saturated aq. NaHCO₃ and brine. After drying the solution over Na₂SO₄, the reaction mixture was concentrated and the resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-5-(5,6-dihydro-8H-[1,2,4]triazolo[4,3-a]pyrazin-7-yl)-pentyl ester (30 mg, 30%) LRMS (M+H⁺) m/z 595.2.

Example 24 Preparation of Isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-5-(2-oxo-piperazin-1-yl-pentyl ester

To a solution of isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-5-oxo-pentyl ester (0.8 g crude mixture, 1.64 mmol) in anhydrous DCE (3 mL) and AcOH (0.1 mL) was added (2-Amino-ethyl)-carbamic acid tert-butyl ester at 24° C. After 10 h of stirring at 24° C., sodium triacetoxyborohydride (1.05 g, 4.92 mmol) was added in one portion. The slurry was stirred for 2 h at 24° C., quenched with methanol and concentrated. The resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give isoquinolin-3-yl-carbamic acid 5-(2-tert-butoxycarbonylamino-ethylamino)-2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-pentyl ester (0.25 g, 25%) LRMS (M+H⁺) m/z 631.2.

To a solution of isoquinolin-3-yl-carbamic acid 5-(2-tert-butoxycarbonylamino-ethylamino)-2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-pentyl ester (0.25 g, 0.40 mmol) in EtOAc (5 mL) and saturated aq. NaHCO₃ (4 mL) was added chloroacetyl chloride (49 mg, 0.43 mmol) at 0° C. After 2 h of stirring at 0° C., phases were separated and organic layers were washed with brine and concentrated, and the resulting residue was re-dissolved in 3 mL of MeOH and treated with 4 M HCl in MeOH (0.105 mL, 0.42 mmol) at 0° C. The mixture was stirred for 2 h at 0° C., and then solid NaHCO₃ (150 mg) was added. After stiffing at 0° C. for another 2 h, the reaction mixture was concentrated and taken up in EtOAc. The resulting organic mixture was washed with brine and dried over Na₂SO₄, and concentrated. The resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O (0.1% TFA buffer). The purified fractions were concentrated, redissolved in EtOAc and washed with saturated aq. NaHCO₃. Removal of the solvent afforded isoquinolin-3-yl-carbamic acid 2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-5-(2-oxo-piperazin-1-yl)-pentyl ester as the free base (37 mg, 17%) LRMS (M+H⁺) m/z 571.2.

Example 25 Preparation of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-3-(1H-imidazol-4-yl)propyl 6-fluoroisoquinolin-3-ylcarbamate

To a solution of (S)-2-(tert-butoxycarbonylamino)-3-(1H-imidazol-4-yl)propanoic acid (1.0 g, 3.92 mmol) in THF (20 mL) was added LAH (2 M, 10 mL, 20 mmol) at 0-5° C. The reaction mixture was stirred at 0-5° C. for 30 min and heat to reflux for 2 h. The reaction mixture was cooled to 0-5° C. and quenched with water (0.8 mL), NaOH (0.8 mL), and water (2.4 mL). The resulting suspension was stirred RT for 30 min and filtered. The filtrate was concentrated to give (S)-3-(1H-imidazol-4-yl)-2-(methylamino)propan-1-ol (400 mg, crude), which was used without further purification. LRMS (M-Boc+H⁺) m/z 156.1.

To a solution of (S)-3-(1H-imidazol-4-yl)-2-(methylamino)propan-1-ol (3.92 mmol) in acetonitrile (10 mL) were added Boc₂O (1.6 g, 7.34 mmol) and DIEA (1.5 mL, 9.06 mmol). The reaction mixture was stirred at RT for 1 h and concentrated to dryness. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-tert-butyl 4-(2-(tert-butoxycarbonyl(methyl)amino)-3-hydroxypropyl)-1H-imidazole-1-carboxylate (260 mg, 19% for two steps). LRMS (M+H⁺) m/z 356.5.

To a solution of (S)-tert-butyl 4-(2-(tert-butoxycarbonyl(methyl)amino)-3-hydroxypropyl)-1H-imidazole-1-carboxylate (260 mg, 0.73 mmol) in toluene (10 mL) was added 6-fluoro-isoquinoline-3-carbonyl azide (174 mg, 0.81 mmol). The reaction mixture was stirred at 100° C. for 30 min, cooled to RT, and concentrated under reduced pressure. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-tert-butyl 4-(2-(tert-butoxycarbonyl(methyl)amino)-3-(6-fluoroisoquinolin-3-ylcarbamoyloxy)propyl)-1H-imidazole-1-carboxylate (280 mg, 71%). LRMS (M+H⁺) m/z 544.2.

To a solution of (S)-tert-butyl 4-(2-(tert-butoxycarbonyl(methyl)amino)-3-(6-fluoroisoquinolin-3-ylcarbamoyloxy)propyl)-1H-imidazole-1-carboxylate (280 mg, 0.51 mmol) in THF (10 mL) was added HCl (4 N in 1,4-dioxane, 2.55 mL, 10.2 mmol). The reaction mixture was stirred at RT for 1 h and concentrated to dryness. The residue was suspended in THF (20 mL). To the suspension were added DIEA (0.27 mL, 1.53 mmol) and 4-nitrophenyl 2-chloro-3-fluorobenzylcarbamate (166 mg, 0.51 mmol). The reaction mixture was stirred at RT for 2 h and concentrated to dryness. The residue was purified on RP-HPLC using a mixture of acetonitrile and water to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-3-(1H-imidazol-4-yl)propyl 6-fluoroisoquinolin-3-ylcarbamate (35 mg, 13%). LRMS (M+H⁺) m/z 529.5.

Example 26 Preparation of (S)-2-((2-chloro-3-fluorobenzyl)(methyl)amino)-3-(pyridin-2-yl)propyl isoquinolin-3-ylcarbamate

To a solution of (S)-2-(tert-butoxycarbonylamino)-3-(pyridin-2-yl)propanoate (1.05 g, 3.96 mmol) in THF (20 mL) was added LAH (2 M in THF, 4.0 mL, 8.0 mmol) at 0° C. The resulting solution was stirred at 0° C. for 30 min and heated to reflux for 2 h. The reaction mixture was cooled and quenched with water (0.32 mL), NaOH (3 N, 0.32 mL), and water (0.96 mL). The resulting suspension was stirred at RT for 30 min. The mixture was filtered and the filtrate was concentrate to give (S)-2-(methylamino)-3-(pyridin-2-yl)propan-1-ol (510 mg, crude), which was used without further purification.

To a solution of (S)-2-(methylamino)-3-(pyridin-2-yl)propan-1-ol (3.93 mmol) in THF (20 mL) was added 4-nitrophenyl 2-chloride-3-fluorobenzylcarbamate (1.29 g, 3.93 mmol). The resulting solution was stirred at RT for 1 h. The solvent was removed and the resulting residue was dissolved in EtOAc (800 mL). The organic mixture was washed with NaOH (1 N, 100 mL×3), HCl (0.5 N, 100 mL), NaHCO₃ (sat.), and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The residue was purified on RP-HPLC using a mixture of acetonitrile and water to give (S)-3-(2-chloro-3-fluorobenzyl)-1-(1-hydroxy-3-(pyridin-2-yl)propan-2-yl)-1-methylurea (250 mg, 18% for two steps). LRMS (M+H⁺) m/z 352.2.

To a solution of (S)-3-(2-chloro-3-fluorobenzyl)-1-(1-hydroxy-3-(pyridin-2-yl)propan-2-yl)-1-methylurea (250 mg, 0.71 mmol) in toluene (10 mL) was added isoquinoline-3-carbonyl azide (142 mg, 0.71 mmol). The resulting solution was stirred at 100° C. for 1 h. The mixture was cooled and concentrated. The residue was purified on RP-HPLC using a mixture of acetonitrile and water to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pent-4-enyl isoquinolin-3-ylcarbamate (277.4 mg, 75%) as white solid. LRMS (M+H⁺) m/z 522.1.

Example 27 Preparation of (S)-5-(2-aminoacetamido)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentyl 6-fluoroisoquinolin-3-ylcarbamate

(S)-5-amino-2-(benzyloxycarbonylamino)pentanoic acid (10.0 g, 37.56 mmol) and ethyl 1,3-dioxoisoindoline-2-carboxylate (9.04 g, 41.28 mmol) in NMP (40.0 mL) were heated to 150° C. for 30 min in 4 microwave reaction tubes. The mixture was diluted with EtOAc (500 mL). The organic mixture was washed with water (100 mL×2) and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure to give an oil, which was redissolved in toluene. To the resulting solution were added paraformaldehyde, PTSA and molecular sieves (3 A) and the mixture was heated to 150° C. for 20 min in a microwave reactor. The reaction mixture was diluted with ether (800 mL), washed with NaHCO₃ and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The residue was purified on silica gel using a mixture of EtOAc and hexanes to give (S)-benzyl 4-(3-(1,3-dioxoisoindolin-2-yl)propyl)-5-oxooxazolidine-3-carboxylate (11.6 g, 76% for 2 steps).

To a solution of (S)-benzyl 4-(3-(1,3-dioxoisoindolin-2-yl)propyl)-5-oxooxazolidine-3-carboxylate (11.6 g, 28.40 mmol) in DCM (30.0 mL) was added Et₃SiH (13.6 mL, 85.3 mmol). The reaction mixture was stirred overnight, concentrated under reduced pressure, and dissolved in THF (100 mL). To the resulting solution was added tert-butyl chloroformate (4.4 mL, 34.08 mmol) and TEA (12.0 mL, 85.2 mmol) at 0° C. The reaction mixture was stirred at RT for 30 min. The precipitate was filtered off and the filtrate was added into a suspension of NaBH₄ in water (1.0 mL) at 0° C. The reaction mixture was stirred at RT for 30 min. LCMS indicated the completion of the reaction. The reaction mixture was acidified to pH 3 by HCl (1N) and extracted with EtOAc (300 mL×2). The combined organic layers were washed with saturated NaHCO₃ and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The residue was purified on silica gel using a mixture of EtOAc and hexanes to give (S)-benzyl 5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl(methyl)carbamate (5.01 g, 45%). LRMS (M+H⁺) m/z 397.3.

To a solution of (S)-benzyl 5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl(methyl)carbamate (5.01 g, 12.65 mmol) in MeOH (100 mL) was added Pd/C (1.0 g). The mixture was transferred to an autoclave reactor, charged with hydrogen (50 psi), and stirred at RT overnight. The mixture was filtered and the filtrate was concentrated under reduced pressure to give (S)-2-(5-hydroxy-4-(methylamino)pentyl)isoindolin (3.2 g, 97%) which was used without purification. LRMS (M+H⁺) m/z 263.1.

To a solution of 4-nitrophenylchloroformate (1.89 g, 9.39 mmol) in THF (20 mL) was added a solution of 2-chloro-3-fluorobenzylamine hydrochloride (1.24 g, 9.39 mmol) and DIEA (3.9 mL, 23.46 mmol). The resulting solution was stirred at RT for 20 min. The reaction mixture was added into a solution of (S)-2-(5-hydroxy-4-(methylamino)pentyl)isoindolin (2.05 g, 7.82 mmol) in THF (10 mL). The resulting solution was stirred at RT overnight. The mixture was concentrated and purified on RP-HPLC using a mixture of acetonitrile and water to give (S)-3-(2-chloro-3-fluorobenzyl)-1-(5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl)-1-methylurea (401 mg, 47%). LRMS (M+H⁺) m/z 448.3.

To a solution of (S)-3-(2-chloro-3-fluorobenzyl)-1-(5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl)-1-methylurea (286 mg, 0.64 mmol) and 6-fluoroisoquinoline-3-carbonyl azide (152 mg, 0.70 mmol) in toluene (5 mL) was heated to 100° C. for 1 h. The reaction mixture was concentrated to dryness. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(1,3-dioxoisoindolin-2-yl)pentyl 6-fluoroisoquinolin-3-ylcarbamate (400 mg, quant.). LRMS (M+H⁺) m/z 618.2.

To a solution of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(1,3-dioxoisoindolin-2-yl)pentyl 6-fluoroisoquinolin-3-ylcarbamate (400 mg, 0.64 mmol) in MeOH (10.0 mL) was added NH₂NH₂ (1.0 mL). The reaction mixture was stirred at RT for 2 h. The mixture was concentrated and re-dissolved in MeOH. The resulting solution was filtered and purified on RP-HPLC using a mixture of acetonitrile and water to give (S)-5-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentyl 6-fluoroisoquinolin-3-ylcarbamate (305 mg, quant.). LRMS (M+H⁺) m/z 506.2.

To a solution of (S)-5-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentyl 6-fluoroisoquinolin-3-ylcarbamate (96 mg, 0.19 mmol), 2-(tert-butoxycarbonylamino)acetic acid (51 mg, 0.29 mmol) and HBTU (110 mg, 0.29 mmol) in DMF (1.0 mL) was added DIEA (63 □L, 0.38 mmol). The mixture was stirred at RT for 30 min. The mixture was filtered and the filtrate was purified by RP-HPLC using a mixture of acetonitrile and water to give (6-Fluoro-isoquinolin-3-yl)-carbamic acid (S)-5-(2-tert-butoxycarbonylamino-acetylamino)-2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-pentyl ester (105 mg, 83%). LRMS (M+Na⁺) m/z 663.2.

To a solution of (6-Fluoro-isoquinolin-3-yl)-carbamic acid (S)-5-(2-tert-butoxycarbonylamino-acetylamino)-2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-pentyl ester (105 mg, 0.16 mmol) in DCM (10.0 mL) was added TFA (1.0 mL). The mixture was stirred at RT for 2 h. The mixture was concentrated and re-dissolved DCM. The DCM layer was washed with K₂CO₃ (2 N), saturated NaHCO₃, and brine, dried over Na₂SO₄, filtered, and concentrated. The residue was purified on silica gel column using a mixture of DCM and MeOH to give (S)-5-(2-aminoacetamido)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentyl 6-fluoroisoquinolin-3-ylcarbamate (71 mg, 79%). LRMS (M+H⁺) m/z 563.2.

Example 28 Preparation of (S,E)-5-(2-carbamoylguanidino)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentyl 6-fluoroisoquinolin-3-ylcarbamate

To a solution of (S)-3-(2-chloro-3-fluorobenzyl)-1-(5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl)-1-methylurea (286 mg, 0.64 mmol) and 6-fluoroisoquinoline-3-carbonyl azide (152 mg, 0.70 mmol) in toluene (5 mL) was heated to 100° C. for 1 h. The reaction mixture was concentrated to dryness. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(1,3-dioxoisoindolin-2-yl)pentyl 6-fluoroisoquinolin-3-ylcarbamate (400 mg, quant.). LRMS (M+H⁺) m/z 618.2.

To a solution of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(1,3-dioxoisoindolin-2-yl)pentyl 6-fluoroisoquinolin-3-ylcarbamate (400 mg, 0.64 mmol) in MeOH (10.0 mL) was added NH₂NH₂ (1.0 mL). The reaction mixture was stirred at RT for 2 h. The mixture was concentrated and re-dissolved in MeOH. The mixture was filtered and purified on RP-HPLC using a mixture of acetonitrile and water to give (S)-5-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentyl 6-fluoroisoquinolin-3-ylcarbamate (305 mg, quant.). LRMS (M+H⁺) m/z 506.2.

To a solution of (S)-5-(2-aminoacetamido)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentyl 6-fluoroisoquinolin-3-ylcarbamate (190 mg, 0.35 mmol) and diphenyl cyanocarbonimidate (83 mg, 0.35 mmol) in DCM (10.0 mL) was added DIEA (0.12 mL, 0.70 mmol). The reaction mixture was stirred at RT for 4 h. The mixture was concentrated under reduced pressure to give (S,Z)-2-(3-(2-chloro-3-fluorophenyl)-N-methylpropanamido)-5-((cyanoimino)(phenoxy)methylamino)pentyl 6-fluoroisoquinolin-3-ylcarbamate, which was used without further purification. LRMS (M+H⁺) m/z 650.2.

To a solution of (S,Z)-2-(3-(2-chloro-3-fluorophenyl)-N-methylpropanamido)-5-((cyanoimino)(phenoxy)methylamino)pentyl 6-fluoroisoquinolin-3-ylcarbamate (100 mg, crude, 0.12 mmol) in MeOH (7 N ammonia, 1.0 mL) was heated at microwave reactor at 110° C. for 20 min. The mixture was filtered and the filtrate was purified by RP-HPLC using a mixture of acetonitrile and water (0.1% TFA buffer). Upon concentration of the mixture. The mixture was purified again with RP-HPLC using a mixture of acetonitrile and water to give (S,E)-5-(2-carbamoylguanidino)-2-(3-(2-chloro-3-fluorophenyl)-N-methylpropanamido)pentyl 6-fluoroisoquinolin-3-ylcarbamate (18 mg, 25%). LRMS (M+H⁺) m/z 591.2.

Example 29 Preparation of (S)-5-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentyl 5-chloropyridin-2-ylcarbamate

To a solution of (S)-3-(2-chloro-3-fluorobenzyl)-1-(5-(1,3-dioxoisoindolin-2-yl)-1-hydroxypentan-2-yl)-1-methylurea (480 mg, 1.07 mmol), 5-chloropicolinic acid (339 mg, 2.15 mmol), and DIEA (0.36 mL, 2.15 mmol) in toluene (10 mL) was added DPPA (0.46 mL, 2.15 mmol). The reaction mixture was heated to 100° C. for 2 h and concentrated to dryness. The residue was purified on RP-HPLC using a mixture of acetonitrile and water to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(1,3-dioxoisoindolin-2-yl)pentyl 5-chloropyridin-2-ylcarbamate (280 mg, 80% pure). LRMS (M+H⁺) m/z 602.2.

To a solution of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(1,3-dioxoisoindolin-2-yl)pentyl 5-chloropyridin-2-ylcarbamate (280 mg, 0.47 mmol) in MeOH (5.0 mL) was added NH₂NH₂ (0.13 mL, 4.7 mmol). The reaction mixture was stirred at RT for 2 h. The mixture was concentrated and re-dissolved in MeOH. The resulting solution was filtered and purified on RP-HPLC using a mixture of acetonitrile and water to give (S)-5-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentyl 5-chloropyridin-2-ylcarbamate (162 mg, 73%). LRMS (M+H⁺) m/z 472.2.

Example 30 Preparation of (2S,4R)-2-((2-chloro-3-fluorobenzyl)(methyl)amino)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate and (2S,4S)-2-((2-chloro-3-fluorobenzyl)(methyl)amino)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate

To a solution of (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)pent-4-en-2-yl(methyl)carbamate (10.5 g, 31.9 mmol) in DCM (100 mL) was added 2,6-lutidine (4.8 mL, 41.4 mmol) followed by TMSOTf (7.5 mL, 41.4 mmol). The resulting solution was stirred at RT for 30 min. The solvent was removed and the remaining residue was dried under vacuum to give (S)-1-(tert-butyldimethylsilyloxy)-N-methylpent-4-en-2-amine, which was used without further purification. LRMS (M+H⁺) m/z 230.2.

To a solution of 4-nitrophenylchloroformate (7.69 g, 38.3 mmol) in THF (20 mL) was added a solution of 2-chloro-3-fluorobenzylamine hydrochloride (6.09 g, 38.3 mmol) and DIEA (7.9 mL, 47.9 mmol) in THF (20 mL). The resulting solution was stirred at RT for 20 min. The reaction mixture was added into a solution of (S)-1-(tert-butyldimethylsilyloxy)-N-methylpent-4-en-2-amine (31.9 mmol) in THF (100 mL). The resulting solution was stirred at RT overnight. The solvent was removed and the resulting residue was re-dissolved in EtOAc (500 mL). The organic mixture was washed with NaOH (1 N, 100 mL×3), HCl (0.5 N, 100 mL), saturated NaHCO₃, and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The residue was purified on silica gel column using a mixture of DCM and MeOH to give (S)-1-(1-(tert-butyldimethylsilyloxy)pent-4-en-2-yl)-3-(2-chloro-3-fluorobenzyl)-1-methylurea (10.08 g, 76%) as a white solid. LRMS (M+H⁺) m/z 415.2.

To a solution of (S)-1-(1-(tert-butyldimethylsilyloxy)pent-4-en-2-yl)-3-(2-chloro-3-fluorobenzyl)-1-methylurea (5.80 g, 10.8 mmol) in MeOH (50 mL) was added HCl (1N, 32.0 mL). The resulting solution was stirred at RT for 30 min. The mixture was partially concentrated and filtered. The filtrate was purified on RP-HPLC using a mixture of acetonitrile and water to give (S)-3-(2-chloro-3-fluorobenzyl)-1-(1-hydroxypent-4-en-2-yl)-1-methylurea (2.0 g, 77%) as a white solid, which was used without further purification. LRMS (M+H⁺) m/z 301.2.

To a solution of (S)-3-(2-chloro-3-fluorobenzyl)-1-(1-hydroxypent-4-en-2-yl)-1-methylurea (1.7 g, 5.65 mmol) in toluene (20 mL) was added isoquinoline-3-carbonyl azide (1.24 g, 6.22 mmol). The resulting solution was stirred at 100° C. for 1 h. The mixture was cooled and the solid was filtered out. The solid was washed with toluene and dry under high vacuum to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pent-4-enyl isoquinolin-3-ylcarbamate (2.50 g, 77%). LRMS (M+H⁺) m/z 471.1.

To a solution of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pent-4-enyl isoquinolin-3-ylcarbamate (1.9 g, 4.03 mmol) in THF (48 mL) and water (12.0 mL) were added 4-methylmorpholine N-oxide (2.36 g, 20.15 mmol) and osmium tetroxide (103.0 mg, 0.4 mmol). The resulting solution was stirred at RT for 2 h. To this mixture was added sodium sulfite (3 g) and the resulting mixture was stirred for 2 h. The solid was then removed by filtration. The filtrate was diluted with ethyl acetate (100 mL). The organic layer was washed with HCl (0.5 N), saturated NaHCO₃, and brine, filtered, and concentrated. The residue was purified by RP-HPLC using a mixture of acetonitrile and water to give (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate (296 mg, 15%), (2S,4S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate (18.3 mg, 9%), and 1 g of mixture. LRMS (M+H⁺) m/z 505.2.

Example 31 Preparation of sodium (2R,4S)-4-(2-chloro-3-fluorobenzyl)(methyl)amino)-2-hydroxy-5-(isoquinolin-3-ylcarbamoyloxy)pentyl phosphate

To a solution of (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate (0.26 g, 0.51 mmol), DIEA (0.51 mL, 3.06 mmol) and DMAP (0.251 g, 2.06 mmol) in anhydrous THF (20 mL) and DCM (30 mL) was added diethyl chlorophorophosphate (0.3 mL, 2.06 mmol) at 0° C. After stirred at RT for 10 min, the mixture was quenched with EtOH. The resulting mixture was diluted with DCM (100 mL). The organic mixture was washed with saturated NaHCO₃, HCL (1 N), saturated NaHCO₃, and brine, dried over Na₂SO₄, filtered, and concentrated. The residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(diethoxyphosphoryloxy)-4-hydroxypentyl isoquinolin-3-ylcarbamate (310 mg, 95%). LRMS (M+H⁺) m/z 641.2.

To a solution of (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(diethoxyphosphoryloxy)-4-hydroxypentyl isoquinolin-3-ylcarbamate (310 mg, 0.64 mmol) in acetonitrile (10 mL) was added TMSI (0.87 mL, 6.4 mmol) at RT. After stirred at RT for 1 h, the reaction was quenched with H₂O and DIEA (0.1 mL, 0.64 mmol). The solvent was removed and the resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O (0.1% HCOOH buffer) to give (2S,4R)-2-(2-chloro-3-fluorobenzyl)(methyl)amino)-4-hydroxy-5-(phosphonooxy)pentyl 6-fluoroisoquinolin-3-ylcarbamate (212 mg, 57%). LRMS (M+H⁺) m/z 585.5.

((2S,4R)-2-((2-chloro-3-fluorobenzyl)(methyl)amino)-4-hydroxy-5-(phosphonooxy)pentyl 6-fluoroisoquinolin-3-ylcarbamate (212 mg, 0.36 mmol) in MeOH (8 mL) was added NaOH (0.1 N, 7.3 mmol) at 0° C. After stirred at 0° C. for 1 h, the mixture was concentrated to give sodium (2R,4S)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-2-hydroxy-5-(isoquinolin-3-ylcarbamoyloxy)pentyl phosphate (235 mg, quant.) as a white solid. LRMS (M−2Na⁺+3H⁺) m/z 585.5.

Example 32 Preparation of (2S,4R)-2-((2,3-difluorobenzyl)(methyl)amino)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate and (2S,4S)-2-((2,3-difluorobenzyl)(methyl)amino)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate

To a solution of 4-nitrophenylchloroformate (7.04 g, 34.9 mmol) in THF (100 mL) was added a solution of 2,3-difluorobenzylamine (4.26 mL, 36.4 mmol) and DIEA (13.2 mL, 75.9 mmol) in THF (20 mL). The resulting solution was stirred at RT for 20 min. The reaction solution was added into a solution of (S)-1-(tert-butyldimethylsilyloxy)-N-methylpent-4-en-2-amine (31.9 mmol) in THF (50 mL). The resulting solution was stirred at RT overnight. The solvent was removed and the resulting residue was re-dissolved in EtOAc (500 mL). The organic mixture was washed with NaOH (1 N, 100 mL×3), HCl (0.5 N, 100 mL), saturated NaHCO₃, and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The residue was purified on silica gel column using a mixture of DCM and MeOH to give (S)-1-(1-(tert-butyldimethylsilyloxy)pent-4-en-2-yl)-3-(2,3-difluorobenzyl)-1-methylurea (6.8 g, 49%) as a white solid. LRMS (M+H⁺) m/z 399.2.

To a solution of (S)-1-(1-(tert-butyldimethylsilyloxy)pent-4-en-2-yl)-3-(2,3-difluorobenzyl)-1-methylurea (3.45 g, 8.65 mmol) in MeOH (60 mL) was added HCl (4 N in dioxane, 11.0 mL). The resulting solution was stirred at RT for 30 min. The mixture was concentrated and re-dissolved in EtOAc. The organic mixture was washed with saturated NaHCO₃ and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure to give (S)-3-(2,3-difluorobenzyl)-1-(1-hydroxypent-4-en-2-yl)-1-methylurea (2.5 g, quant.) as a white solid, which was used without further purification. LRMS (M+H⁺) m/z 285.2.

To a solution of (S)-3-(2,3-difluorobenzyl)-1-(1-hydroxypent-4-en-2-yl)-1-methylurea (2.5 g, 8.65 mmol) in toluene (20 mL) was added isoquinoline-3-carbonyl azide (2.46 g, 8.65 mmol). The resulting solution was stirred at 100° C. for 1 h. The mixture was cooled and concentrated to half volume followed by addition of hexanes and DCM to give precipitate. The mixture was filtered and the solid was washed with hexanes to give (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)pent-4-enyl isoquinolin-3-ylcarbamate (3.42 g, quant.). LRMS (M+H⁺) m/z 455.2.

To a solution of (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)pent-4-enyl isoquinolin-3-ylcarbamate (3.42 g, 7.52 mmol) in THF (100 mL) and water (25.0 mL) were added 4-methylmorpholine N-oxide (4.4 g, 37.6 mmol) and osmium tetroxide (254.2 mg, 0.75 mmol). The resulting solution was stirred overnight. To this mixture was added sodium sulfite (3 g) and the mixture was stirred for 2 h. The solid was then removed by filtration. The filtrate was diluted with ethyl acetate (200 mL). The organic layer was washed with HCl (0.5 N), saturated NaHCO₃, and brine, filtered, and partially concentrated. The mixture was filtered and the solid was collected and dried to give a mixture of (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate and (2S,4S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate (1 g) as 1:2 ratio. The filtrate was concentrated and purified by RP-HPLC using a mixture of acetonitrile and water to give (2S,4R)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate (14 mg), (2S,4S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate (10 mg), and a mixture of both (300 mg). LRMS (M+H⁺) m/z 489.2.

Example 33 Preparation of Sodium (2R,4S)-4-((2,3-difluorobenzyl)(methyl)amino)-2-hydroxy-5-(isoquinolin-3-ylcarbamoyloxy)pentyl phosphate

To a solution of (2S,4R)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate (0.245 g, 0.50 mmol), DIEA (0.17 mL, 1.0 mmol), and DMAP (0.122 g, 1.0 mmol) in anhydrous THF (12 mL) was added dimethyl chlorophorophosphate (0.11 mL, 1.0 mmol) at 0° C. After stirred at RT for 1 h, an additional dimethyl chlorophorophosphate (0.27 mL, 2.51 mmol) was added at 0° C. The reaction mixture was stirred for 30 min and quenched with MeOH. The resulting mixture was diluted with EtOAc (100 mL). The organic mixture was washed with saturated NaHCO₃, HCL (1 N), saturated NaHCO₃, and brine, dried over Na₂SO₄, filtered, and concentrated. The residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (2S,4R)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(dimethoxyphosphoryloxy)-4-hydroxypentyl isoquinolin-3-ylcarbamate (150 mg, 50%). LRMS (M+H⁺) m/z 597.2.

(2S,4R)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(dimethoxyphosphoryloxy)-4-hydroxypentyl isoquinolin-3-ylcarbamate (150 mg, 0.25 mmol) in acetonitrile (10 mL) was added TMSI (0.14 mL, 1.0 mmol) at 0° C. After stirred at RT for 10 min, the reaction was quenched with MeOH. The solvent was removed and the resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O (0.1% HCOOH buffer) to give (2S,4R)-2-((2-chloro-3-fluorobenzyl)(methyl)amino)-4-hydroxy-5-(phosphonooxy)pentyl isoquinolin-3-ylcarbamate (100 mg, 70%). LRMS (M+H⁺) m/z 569.2.

((2S,4R)-2-(2,3-fluorobenzyl)(methyl)amino)-4-hydroxy-5-(phosphonooxy)pentyl isoquinolin-3-ylcarbamate (100 mg, 0.176 mmol) in MeOH (4 mL) was added NaOH (0.1 N, 3.6 mL, 0.36 mmol) at 0° C. After stirred at 0° C. for 1 h, the mixture was concentrated to give sodium (2R,4S)-4-(3-(2,3-difluorobenzyl)-1-methylureido)-2-hydroxy-5-(isoquinolin-3-ylcarbamoyloxy)pentyl phosphate (100.1 mg, 93%) as a white solid. LRMS (M−2Na+3H⁺) m/z 569.5.

Example 34 Preparation of Sodium (2S,4S)-4-((2,3-difluorobenzyl)(methyl)amino)-2-hydroxy-5-(isoquinolin-3-ylcarbamoyloxy)pentyl phosphate

To a solution of (2S,4S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate (0.61 g, 1.23 mmol), DIEA (0.41 mL, 2.45 mmol), and DMAP (0.30 g, 2.46 mmol) in anhydrous THF (20 mL) was added dimethyl chlorophorophosphate (0.13 mL, 1.23 mmol) at 0° C. After stirred at RT for 1 h, an additional dimethyl chlorophorophosphate (0.66 mL, 6.15 mmol) was added at 0° C. The reaction mixture was stirred for 30 min and quenched with MeOH. The mixture was diluted with EtOAc (100 mL). The organic mixture was washed with saturated NaHCO₃, HCL (1 N), saturated NaHCO₃, water and brine, dried over Na₂SO₄, filtered, and concentrated. The residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (2S,4S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(dimethoxyphosphoryloxy)-4-hydroxypentyl isoquinolin-3-ylcarbamate (161 mg, 22%). LRMS (M+H⁺) m/z 597.2.

(2S,4S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(dimethoxyphosphoryloxy)-4-hydroxypentyl isoquinolin-3-ylcarbamate (161 mg, 0.27 mmol) in acetonitrile (5 mL) was added TMSI (0.15 mL, 1.08 mmol) at 0° C. After stirred at RT for 10 min, the reaction was quenched with MeOH. The solvent was removed and the resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O (0.1% HCOOH buffer) to give (2S,4S)-2-((2-chloro-3-fluorobenzyl)(methyl)amino)-4-hydroxy-5-(phosphonooxy)pentyl isoquinolin-3-ylcarbamate (70 mg, 46%). LRMS (M+H⁺) m/z 569.2.

((2S,4S)-2-(2,3-fluorobenzyl)(methyl)amino)-4-hydroxy-5-(phosphonooxy)pentyl isoquinolin-3-ylcarbamate (100 mg, 0.176 mmol) in MeOH (4 mL) was added NaOH (0.1 N, 3.6 mL, 0.36 mmol) at 0° C. After stirred at 0° C. for 1 h, the mixture was concentrated to give sodium (2S,4S)-4-(3-(2,3-difluorobenzyl)-1-methylureido)-2-hydroxy-5-(isoquinolin-3-ylcarbamoyloxy)pentyl phosphate (80 mg, quant.) as a white solid. LRMS (M−2Na⁺+3H⁺) m/z 569.5.

Example 35 Preparation of (2S,4S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl 6-fluoroisoquinolin-3-ylcarbamate and (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl 6-fluoroisoquinolin-3-ylcarbamate

A solution of crude (2S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl 6-fluoroisoquinolin-3-ylcarbamate (0.07 g) in DCM (1 mL) was loaded onto a TLC Silica gel 60 F254 (20×20 cm) plate and developed with a mixture of DCM and methanol (20:1). The top layer was collected and stirred in methanol (50 mL) for 10 min. After filtration, the filtrate was concentrated to give (2S,4S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl 6-fluoroisoquinolin-3-ylcarbamate (0.01 g, 14.3%). LRMS (M+H⁺) m/z 523.2. The same process was applied to the bottom layer to give (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl 6-fluoroisoquinolin-3-ylcarbamate (27 mg, 38.6%). LRMS (M+H⁺) m/z 523.2.

Example 36 Preparation of (2S)-2-((2,3-difluorobenzyl)(methyl)amino)-5-dihydroxypentyl isoquinolin-3-ylcarbamate

To a solution of 4-nitrophenylchloroformate (6.66 g, 33.0 mmol) in THF (100 mL) was added a solution of 2,3-difluorobenzylamine (4.04 mL, 34.5 mmol) and DIEA (17.5 mL, 100.5 mmol) in THF (20 mL). The resulting solution was stirred at RT for 20 min. The reaction solution was added into a solution of (S)-methyl 5-(tert-butyldimethylsilyloxy)-4-(methylamino)pentanoate (28.8 mmol) in THF (30 mL). The resulting solution was stirred at RT for 1 h. The solvent was removed and the resulting residue was re-dissolved in EtOAc (500 mL). The organic mixture was washed with NaOH (1 N, 100 mL×3), HCl (0.5 N, 100 mL), saturated NaHCO₃, and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The residue was purified on silica gel column using a mixture of DCM and MeOH to give (S)-methyl 5-(tert-butyldimethylsilyloxy)-4-(3-(2,3-difluorobenzyl)-1-methylureido)pentanoate (9.7 g, 76% for three steps) as an oil. LRMS (M+H⁺) m/z 445.2.

To a solution of (S)-methyl 5-(tert-butyldimethylsilyloxy)-4-(3-(2,3-difluorobenzyl)-1-methylureido)pentanoate (9.7 g, 21.6 mmol) in MeOH (40 mL) was added HCl (4 N in dioxane, 5.4.0 mL, 21.6 mmol). The resulting solution was stirred at RT for 1 h. The mixture was concentrated and re-dissolved in EtOAc. The organic mixture was washed with saturated NaHCO₃ and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure to give (S)-methyl 4-(3-(2,3-difluorobenzyl)-1-methylureido)pentanoate (6.84 g, crude) as a white solid, which was used without further purification. LRMS (M+H⁺) m/z 331.2.

To a solution of (S)-methyl 4-(3-(2,3-difluorobenzyl)-1-methylureido)pentanoate (2.23 g, 6.75 mmol) in toluene (20 mL) was added isoquinoline-3-carbonyl azide (1.33 g, 6.75 mmol). The resulting solution was stirred at 100° C. for 1 h. The mixture was cooled and concentrated. The residue was purified on silica gel to give (S)-methyl 4-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(isoquinolin-3-ylcarbamoyloxy)pentanoate (2.48 g, 73% for two steps). LRMS (M+H⁺) m/z 501.2.

To a solution of (S)-methyl 4-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(isoquinolin-3-ylcarbamoyloxy)pentanoate (1.0 g, 2.0 mmol) in THF (10 mL) was added LAH (2.0 M in THF, 1.5 mL, 3.0 mmol) at 0° C. and stirred at 0° C. for 20 min. The mixture was quenched with H₂O (0.12 mL), NaOH (3 N, 0.12 mL), and H₂O (0.36 mL) and the resulting suspension was stirred at RT for 30 min and filtered. The filtrate was concentrated and the residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-5-hydroxypentyl isoquinolin-3-ylcarbamate (0.52 g, 55%). LRMS (M+H⁺) m/z 473.2.

Example 37 Preparation of sodium (S)-4-((2,3-difluorobenzyl)(methyl)amino)-5-(isoquinolin-3-ylcarbamoyloxy)pentyl phosphate

Method A:

To a solution of (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-5-hydroxypentyl isoquinolin-3-ylcarbamate (0.52 g, 1.11 mmol), DIEA (0.96 mL, 5.52 mmol), and DMAP (0.27 g, 2.21 mmol) in anhydrous DCM (10 mL) was added dimethyl chlorophorophosphate (0.36 mL, 3.36 mmol) at RT After stirred at RT for 15 min, the reaction mixture was quenched with MeOH. The mixture was diluted with EtOAc (100 mL). The organic mixture was washed with saturated NaHCO₃, HCl (1 N), saturated NaHCO₃, and brine, dried over Na₂SO₄, filtered, and concentrated to give (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(dimethoxyphosphoryloxy)pentyl isoquinolin-3-ylcarbamate (626 mg, 98%), which was used without purification. LRMS (M+H⁺) m/z 581.2.

(S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(dimethoxyphosphoryloxy)pentyl isoquinolin-3-ylcarbamate (531 mg, 0.91 mmol) in acetonitrile (18 mL) was added TMSI (0.50 mL, 3.66 mmol) at 0° C. After stirred at RT for 10 min, the reaction was quenched with MeOH. The solvent was removed and the resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O (0.1% HCOOH buffer) to give (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(phosphonooxy)pentyl isoquinolin-3-ylcarbamate (261 mg, 52%). LRMS (M+H⁺) m/z 553.5.

(S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(phosphonooxy)pentyl isoquinolin-3-ylcarbamate (261 mg, 0.472 mmol) in MeOH (10 mL) was added NaOH (0.1 N, 9.2 mL, 0.92 mmol) at 0° C. After stirred at 0° C. for 1 h, the mixture was concentrated to give sodium (S)-4-((2,3-difluorobenzyl)(methyl)amino)-5-(isoquinolin-3-ylcarbamoyloxy)pentyl phosphate (260 mg, 88%) as a white solid. LRMS (M+H⁺) m/z 585.5.

Method B:

To a solution of (S)-methyl 4-(tert-butoxycarbonylamino)-5-(tert-butyldimethylsilyloxy)pentanoate (40 g, 0.111 mol) in THF (100 mL) and MeOH (5.0 mL) was added LiBH₄ (2M in THF, 56.0 mL, 0.112 mol) at 0° C. The reaction mixture was stirred at RT for 2 h. The reaction mixture was cooled to 0° C. and slowly quenched with saturated NaHCO₃ solution. The resulting mixture was stirred RT overnight and filtered. The solid was washed with EtOAc. The combined filtrate was diluted with an additional EtOAc (200 mL). The organic layer was washed with water and brine, dried over Na₂SO₄, filtered, and concentrated to give (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)-5-hydroxypentan-2-ylcarbamate (39.5 g), which was used without further purification. LRMS (M+Na⁺) m/z 356.4.2.

To a solution of (S)-methyl 4-(tert-butoxycarbonyl(methyl)amino)-5-(tert-butyldimethylsilyloxy)pentanoate (111 mmol) and pyridine (150 mL, 1.662 mol) in THF (500 mL) was added acetyl chloride (150 mL, 333.2 mmol) at 0° C. The resulting mixture was stirred at RT for 1 h. The solvent was removed and the remaining residue was diluted with EtOAc. The organic mixture was washed with water and brine, dried over Na₂SO₄, filtered, and concentrated. The residue was purified on silica gel column to give (S)-4-(tert-butoxycarbonylamino)-5-(tert-butyldimethylsilyloxy)pentyl acetate (39.6 g, 95%). LRMS (M+H⁺-Boc) m/z 276.2.

To a solution of (S)-4-(tert-butoxycarbonylamino)-5-(tert-butyldimethylsilyloxy)pentyl acetate (48.2 g, 0.124 mol) and MeI (23.2 mL, 0.372 mol) in DMF (500 mL) was added sodium hydride (60%, 9.9 g, 0.248 mol) at 0° C. The resulting mixture was stirred at 0° C. for 2½ h and LC-MS indicated the reaction was completed. The reaction was quenched with saturated NH₄Cl solution and diluted with EtOAc. The organic layer was washed with water and brine, dried over Na₂SO₄, filtered, and concentrated to give (S)-4-(tert-butoxycarbonyl(methyl)amino)-5-(tert-butyldimethylsilyloxy)pentyl acetate (51 g, crude). LRMS (M+H⁺-Boc) m/z 290.2.

To a solution of (S)-4-(tert-butoxycarbonyl(methyl)amino)-5-(tert-butyldimethylsilyloxy)pentyl acetate (0.124 mol) in THF (200 mL) and MeOH (50 mL) was added sodium hydroxide (2 N, 93 mL, 0.186 mol) at RT The reaction was stirred at RT for 2 h and LC-MS indicated the reaction was completed. The reaction mixture was diluted with EtOAc and the organic layer was washed with water and brine, dried over Na₂SO₄, filtered, and concentrated. The resulting residue was purified on silica gel column using a mixture of hexanes and EtOAc to give (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)-5-hydroxypentan-2-yl(methyl)carbamate (37.9 g, 88%). LRMS (M+H⁺-Boc) m/z 248.2.

To a solution of (S)-methyl 4-(tert-butoxycarbonyl(methyl)amino)-5-(tert-butyldimethylsilyloxy)pentanoate (37.9 g, 109.2 mmol) in DCM (200 mL) was added 2,6-lutidine (25.3 mL, 218.4 mmol) followed by TMSOTf (29.6 mL, 163.8 mmol). The resulting solution was stirred at RT for 1 h. The solvent was removed and the remaining residue was diluted with EtOAc. The organic mixture was washed with water and brine, dried over Na₂SO₄, filtered, and concentrated to give (S)-5-(tert-butyldimethylsilyloxy)-4-(methylamino)pentan-1-ol, which was used without further purification. LRMS (M+H⁺) m/z 248.2.

To a solution of (S)-5-(tert-butyldimethylsilyloxy)-4-(methylamino)pentan-1-ol (109.2 mmol) in THF (200 mL) was added 4-nitrophenyl 2,3-difluorobenzylcarbamate (43.72 g, 142.0 mmol). The resulting solution was stirred at RT for 1 h. The solvent was removed and the resulting residue was dissolved in EtOAc (800 mL). The organic mixture was washed with NaOH (1 N, 100 mL×3), HCl (0.5 N, 100 mL), NaHCO₃ (sat.), and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The residue was purified on silica gel column using a mixture of EtOAC and hexanes to give (S)-1-(1-(tert-butyldimethylsilyloxy)-5-hydroxypentan-2-yl)-3-(2,3-difluorobenzyl)-1-methylurea (35.1 g, 76%) as a pale yellow oil. LRMS (M+H⁺) m/z 417.2.

To a solution of (S)-1-(1-(tert-butyldimethylsilyloxy)-5-hydroxypentan-2-yl)-3-(2,3-difluorobenzyl)-1-methylurea-(tert-butyldimethylsilyloxy)-4-(3-(2,3-difluorobenzyl)-1-methylureido)pentanoate (6.1 g, 14.66 mmol) in THF (20 mL) was added tetrazole (0.34 M in acetonitrile, 172.0 mL, 58.64 mmol) followed by addition of di-tert-butyl diisopropylphosphoramidite (9.3 mL, 29.32 mmol) at RT The resulting solution was stirred at RT for 2 h. To this mixture was added MCPBA (70%, 7.3 g, 29.32 mmol) at RT. The reaction mixture was stirred at RT overnight and quenched with Na₂SO₃. The mixture was filtered and the filtrate was concentrated and dissolved in EtOAc. The organic mixture was washed with NaOH (1 N×2), NaHCO₃ (sat.), and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-di-tert-butyl 5-(tert-butyldimethylsilyloxy)-4-(3-(2,3-difluorobenzyl)-1-methylureido)pentyl phosphate (4.1 g, 54%). LRMS (M+H⁺⁻2 ^(t)Bu) m/z 491.2.

To a solution of (S)-di-tert-butyl 5-(tert-butyldimethylsilyloxy)-4-(3-(2,3-difluorobenzyl)-1-methylureido)pentyl phosphate (4.1 g, 7.95 mmol) in THF (40 mL) was added TBAF (1.0 M in THF, 8.0 mL, 8.0 mmol). The resulting solution was stirred at RT for 1 h. The mixture was quenched with sat. NH₄Cl and diluted with EtOAc. The organic layer was washed with sat. NH₄Cl (×2) and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-di-tert-butyl 4-(3-(2,3-difluorobenzyl)-1-methylureido)-5-hydroxypentyl phosphate (2.52 g, 61%) as a colorless oil. LRMS (M+H⁺⁻2 ^(t)Bu) m/z 383.0.

To a solution of (S)-di-tert-butyl 4-(3-(2,3-difluorobenzyl)-1-methylureido)-5-hydroxypentyl phosphate (2.52 g, 4.88 mmol) in toluene (100 mL) were added isoquinoline-3-carbonyl azide (1.2 g, 5.86 mmol) and DIEA (1.2 mL, 7.32 mmol). The resulting solution was stirred at 100° C. for 1 h. The mixture was cooled and concentrated. The residue was purified on silica gel column using a mixture of EtOAc and hexanes (0.1% TEA buffer) to give (S)-methyl 4-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(isoquinolin-3-ylcarbamoyloxy)pentanoate (1.95 g, 60%). LRMS (M+H⁺) m/z 665.2.

To a solution of (S)-methyl 4-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(isoquinolin-3-ylcarbamoyloxy)pentanoate (1.65 g, 2.48 mmol) in MeOH was added HCl (6 N in MeOH/water, 8 mL, 48 mmol) at RT and stirred at RT for 30 min. The mixture was concentrated to almost dryness, cooled to 0° C., and adjusted pH to 2 using NaOH (1 N). The resulting precipitate was collected and dried to give (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(phosphonooxy)pentyl (1.37 g, 99.8%). LRMS (M+H⁺) m/z 553.5.

To a solution of (S)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-5-(phosphonooxy)pentyl isoquinolin-3-ylcarbamate (2.50 g, 4.54 mmol) in MeOH (100 mL) was added NaOH (0.1 N, 90.7 mL, 9.07 mmol) at 0° C. After stirred at 0° C. for 1 h, the mixture was concentrated to give sodium (S)-4-((2,3-difluorobenzyl)(methyl)amino)-5-(isoquinolin-3-ylcarbamoyloxy)pentyl phosphate (2.15 g, 79%) as a white solid. LRMS (M−2Na⁺+3H⁺) m/z 553.5.

Example 38 Preparation of sodium (S)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(6-fluoroisoquinolin-3-ylcarbamoyloxy)-2,2-dimethylpentyl phosphate

To a solution of (S)-3,3-dimethyl-dihydropyrrolo[1,2-c]oxazol-5(1H,3H,6H)-one (3.6 g, 23.2 mmol) and iodomethane (1.74 mL, 27.9 mmol) in THF (100 mL) was added LDA (2 M in THF, 14 mL, 28 mmol) at −76° C. After stirring at −76° C. for 4 h, the reaction mixture was added an additional iodomethane (1.86 mL, 30 mmol) in THF (100 mL) and LDA (2 M in THF, 15 mL, 30 mmol). The resulting mixture was stirred at −76° C. for 4 h, warmed to RT, stirred at RT for 4 days, and quenched with saturated NH₄Cl solution. The resulting mixture was diluted with EtOAc. The organic layer was washed with water and brine, dried over Na₂SO₄, filtered, and concentrated. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-3,3,6,6-tetramethyl-dihydropyrrolo[1,2-c]oxazol-5(1H,3H,6H)-one (3.1 g, 73%). LRMS (M+H⁺) m/z 184.1.

To a solution of (S)-3,3,6,6-tetramethyl-dihydropyrrolo[1,2-c]oxazol-5(1H,3H,6H)-one in methanol (20 mL) was added HCl (4 N in 1,4-dioxane, 10 mL, 40 mmol). The reaction mixture was stirred at RT for 30 min, concentrated to dryness, and re-dissolved in DCM (50 mL). To the resulting solution were added imidazole (1.5 g, 22 mmol) and TBS-Cl (2.8 g, 18.6 mmol) respectively. The mixture was stirred at RT overnight and filtered. The filtrate was concentrated and the residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-5-((tert-butyldimethylsilyloxy)methyl)-3,3-dimethylpyrrolidin-2-one (3.1 g, 71.2%). LRMS (M+H⁺) m/z 258.3.

To a solution of (S)-5-((tert-butyldimethylsilyloxy)methyl)-3,3-dimethylpyrrolidin-2-one (3.1 g, 12.1 mmol) and DMAP (2.7 g, 21.8 mmol) in THF (50 mL) was added Boc₂O (4.4 g, 20 mmol). The reaction mixture was stirred at RT for 3 h and concentrated. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-tert-butyl 5-((tert-butyldimethylsilyloxy)methyl)-3,3-dimethyl-2-oxopyrrolidine-1-carboxylate (4.3 g, quant.). LRMS (M-Boc+H⁺) m/z 258.2.

To a solution (S)-tert-butyl 5-((tert-butyldimethylsilyloxy)methyl)-3,3-dimethyl-2-oxopyrrolidine-1-carboxylate (2.7 g, 7.56 mmol) in THF (27 mL) and water (3 mL) was added LiOH (1 N, 15.2 mL, 15.2 mmol). The reaction mixture was stirred at RT overnight and concentrated. The residue was dissolved in water (20 mL), acidified with 10% citric acid to pH 6-7, and extracted with EtOAc. The organic layer was dried over Na₂SO₄, filtered, and concentrated to give (S)-4-(tert-butoxycarbonylamino)-5-(tert-butyldimethylsilyloxy)-2,2-dimethylpentanoic acid (2.6 g, 91.7%), which was used without further purification. LRMS (M-Boc+H⁺) m/z 276.2.

To a solution of (S)-4-(tert-butoxycarbonylamino)-5-(tert-butyldimethylsilyloxy)-2,2-dimethylpentanoic acid (2.5 g, 6.7 mmol) and TEA (1.9 mL, 13.4 mmol) in THF (50 mL) was added isobutyl chloroformate (1.1 mL, 8.04 mmol) at 0-5° C. The reaction mixture was stirred at 0-5° C. for 15 min and filtered. To the filtrate was added a suspension of NaBH₄ (0.5 g, 13.4 mmol) in water (5 mL) at 0-5° C. The reaction mixture was stirred at 0-5° C. for 30 min, quenched with saturated NH₄Cl solution, and extracted with EtOAc (200 mL). The organic layer was washed with water and brine, dried over Na₂SO₄, filtered, and concentrated. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)-5-hydroxy-4,4-dimethylpentan-2-ylcarbamate (2.0 g, 83.1%). LRMS (M+H⁺-Boc) m/z 262.2.

To a solution of (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)-5-hydroxy-4,4-dimethylpentan-2-yl(methyl)carbamate (1.23 g, 3.27 mmol) in THF (20 mL) were added pyridine (0.79 mL) and acetyl chloride (0.386 g, 4.91 mmol). The reaction mixture was stirred at RT overnight and filtered. The filtrate was concentrated to give (S)-4-(tert-butoxycarbonyl(methyl)amino)-5-(tert-butyldimethylsilyloxy)-2,2-dimethylpentyl acetate (1.36 g, crude), which was used without further purification. LRMS (M-Boc+H⁺) m/z 318.2

To a solution of (S)-4-(tert-butoxycarbonyl(methyl)amino)-5-(tert-butyldimethylsilyloxy)-2,2-dimethylpentyl acetate (3.27 mmol) in THF (100 mL) was added TBAF (1.0 M, 16.3 mL, 16.3 mmol). The reaction mixture was stirred at RT for 1 h and concentrated to dryness. The residue was dissolved in EtOAc. The organic mixture was washed with 10% citric acid, saturated NaHCO₃, and brine, dried over Na₂SO₄, filtered, and concentrated to give (S)-4-(tert-butoxycarbonyl(methyl)amino)-5-hydroxy-2,2-dimethylpentyl (0.95 g, crude), which was sued without further purification. LRMS (M-Boc+H⁺) m/z 204.1

To a solution of (S)-4-(tert-butoxycarbonyl(methyl)amino)-5-hydroxy-2,2-dimethylpentyl (3.27 mmol) in toluene (20 mL) was added 6-fluoroisoquinoline-3-carbonyl azide (0.83 g, 3.84 mmol). The reaction mixture was stirred at 100° C. for 30 min, cooled, and concentrated. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-4-(tert-butoxycarbonyl(methyl)amino)-5-(6-fluoroisoquinolin-3-ylcarbamoyloxy)-2,2-dimethylpentyl acetate (1.5 g, 93% for three steps). LRMS (M+H⁺) m/z 492.5

To a solution of (S)-4-(tert-butoxycarbonyl(methyl)amino)-5-(6-fluoroisoquinolin-3-ylcarbamoyloxy)-2,2-dimethylpentyl acetate (1.9 g, 3.8 mmol) in THF (50 mL) was added HCl (4 N in 1,4-dioxane, 19 mL, 76 mmol). The reaction mixture was stirred at RT for 1 h and concentrated to dryness. The residue was suspended in THF (100 mL). To the suspension were added DIEA (2.0 mL, 11.4 mmol) and 4-nitrophenyl 2-chloro-3-fluorobenzylcarbamate (1.2 g, 3.8 mmol). The reaction mixture was stirred at RT for 2 h and concentrated. The residue was purified on RP-HPLC using a mixture of acetonitrile and water to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-hydroxy-4,4-dimethylpentyl 6-fluoroisoquinolin-3-ylcarbamate (1.1 g, 53%). LRMS (M+H⁺) m/z 535.5

To a solution of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-hydroxy-4,4-dimethylpentyl 6-fluoroisoquinolin-3-ylcarbamate (0.45 g, 0.84 mmol), DIEA (0.73 mL, 4.2 mmol), and DMAP (1.02 g, 8.4 mmol) in anhydrous DCM (20 mL) was added dimethyl chlorophorophosphate (0.72 mL, 6.72 mmol) at RT After stirring at RT for 30 min, the reaction mixture was added an additional portion of dimethyl chlorophorophosphate (0.103 mL, 0.956 mmol) and DIEA (0.167 mL, 0.956 mmol). The reaction mixture was monitored by LC/MS. Upon the completion of the reaction, the mixture was quenched with MeOH (10 mL). The solvent was removed and the resulting residue was dissolved in EtOAc (100 mL). The organic mixture was washed with saturated NaHCO₃, water, and brine, dried over Na₂SO₄, filtered, and concentrated. The resulting residue was purified on RP-HPLC using a mixture of acetonitrile and water to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(dimethoxyphosphoryloxy)-4,4-dimethylpentyl 6-fluoroisoquinolin-3-ylcarbamate (280 mg, 52%). LRMS (M+H⁺) m/z 643.6.

To a solution of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(dimethoxyphosphoryloxy)-4,4-dimethylpentyl 6-fluoroisoquinolin-3-ylcarbamate (0.5 g, 0.79 mmol) in acetonitrile (50 mL) was added TMSI (0.848 mL, 6.23 mmol) at 0° C. After stirred at 0° C. for 30 min, the reaction was quenched with MeOH. The solvent was removed and the resulting residue was purified on RP-HPLC using a mixture of acetonitrile and water (0.1% HCOOH buffer) to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,4-dimethyl-5-(phosphonooxy)pentyl 6-fluoroisoquinolin-3-ylcarbamate (340 mg, 71.1%). LRMS (M+H⁺) m/z 615.5.

To a solution of S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,4-dimethyl-5-(phosphonooxy)pentyl 6-fluoroisoquinolin-3-ylcarbamate (340 mg, 0.55 mmol) in MeOH (30 mL) was added NaOH (0.1 N, 10.8 mL, 1.08 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 10 min and concentrated. The residue was dissolved in small amount of water and lyophilized to give sodium (S)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(6-fluoroisoquinolin-3-ylcarbamoyloxy)-2,2-dimethylpentyl phosphate (343 mg, 94.1%) as white solid. LRMS (M−2Na⁺+3H⁺) m/z 615.5.

Example 39 Preparation of di-tert-butyl phosphorobromidate

A 500 mL 3-neck flask equipped with dropping funnel and thermometer was charged with carbon tetrabromide (16.58 g, 50 mmol), benzyltriethylammonium chloride (1.14 g, 5.0 mmol) and dichloromethane (50 mL). A 20% w/w NaOH solution (50 mL) was added with vigorous stirring, followed by dropwise addition of a solution of di-tert-butylphosphite (20 g, 100 mmol) in dichloromethane (20 mL), the rate of addition was controlled to keep the temperature of reaction mixture not to exceed to 25° C. After addition of phosphite, the mixture was further stirred at room temperature for 3 h, diluted with dichloromethane (20 mL) and separated. The organic phase was washed with saturated sodium bisulfite, water, brine, dried (Na₂SO₄), filtered and concentrated at RT. After removing the solvent, the residue was further pumped in vacuo for 1 h to give di-tert-butyl phosphorobromidate as a colorless oil (23.5 g, 86%).

Example 40 Preparation of 1-((2S,4R)-1-(tert-butyldimethylsilyloxy)-4,5-dihydroxypentan-2-yl)-3-(2-chloro-3-fluorobenzyl)-1-methylurea

Method A

A 2 L 3-neck RBF was charged with 4-nitrophenylchloroformate (19.3 g, 96 mmol) and THF (400 mL) under N₂ and chilled to 0° C. in ice bath. To this mixture was added a solution of 2,3-difluorobenzylamine (14.2 g, 92 mmol) and DIEA (17.4 mL, 100 mmol) in one portion. The reaction mixture was stirred at 0° C. for 5 min and then an LC/MS or TLC was taken to confirm consumption of the starting material and presence of the nitrophenyl intermediate. A solution of [(S)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-but-3-enyl]-methyl-amine (76 mmol) in THF (150 mL) was quickly added in one portion to the reaction mixture followed by DIEA (31.7 mL, 182 mmol). The reaction mixture was allowed to warm up to RT for approximately 2 h. The solvent was removed. The crude was diluted with ethyl acetate (1 L), washed with NaOH (1N, 500 mL×4) and brine, dried over sodium sulfate, filtered, and concentrated under reduced pressure. The crude oil was purified on silica gel using a gradient of 0 to 30% ethyl acetate in hexanes to obtain (S)-1-(1-(tert-butyldimethylsilyloxy)pent-4-en-2-yl)-3-(2,3-difluorobenzyl)-1-methylurea (26.1 g, 70%) as a white solid.

To a mixture of t-BuOH (300 mL) and water (300 mL) were added K₂CO₃ (17.0 g, 123 mmol,), (DHQD)₂Pyr (361 mg, 0.41 mmol), K₂OsO₂(OH)₄(151 mg, 0.41 mmol), K₃FeCN₆ (40.5 g, 123 mmol) at RT The mixture was stirred at RT for 2 h and then cooled to 0° C. To the mixture was added a suspension of (S)-1-(1-(tert-butyldimethylsilyloxy)pent-4-en-2-yl)-3-(2-chloro-3-fluorobenzyl)-1-methylurea (17.0 g, 41 mmol) in 100 mL of t-BuOH/water (1:1), and the reaction was stirred at 0° C. overnight. LC-MS indicted the reaction was completed, Na₂S₂O₃.5H₂O (30.6 g, 123 mmol) was added to the reaction, and the reaction was stirred at RT for 30 min. The mixture was diluted with ethyl acetate (1 L), washed with water (250 mL×2) and brine (250 mL), dried over Na₂SO₄, and filtered. The filtrate was concentrated and purified on silica gel to give 1-((2S,4R)-1-(tert-butyldimethylsilyloxy)-4,5-dihydroxypentan-2-yl)-3-(2-chloro-3-fluorobenzyl)-1-methylurea (10.1 g, 55%) as a colorless oil.

To a solution of the 1-((2S,4R)-1-(tert-butyldimethylsilyloxy)-4,5-dihydroxypentan-2-yl)-3-(2-chloro-3-fluorobenzyl)-1-methylurea 1 (4.5 g, 10.0 mmol) in DMF (170 mL) were added 2,2-dimethoxypropane (12.45 mL, 100.0 mmol) and PPTS (0.050 g, 0.02 mmol) at 0° C. After 1 h the reaction was warmed up to RT and stirred for an additional 2.5 h. The crude reaction mixture was then added into a saturated aqueous solution of NaHCO₃ (350 mL) and extracted with EtOAc (3×300 mL). Combined organic layers were washed with Brine (2×400 mL) and dried over MgSO₄. The solution was then concentrated to give 1-((S)-1-(tert-butyldimethylsilyloxy)-3-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)propan-2-yl)-3-(2-chloro-3-fluorobenzyl)-1-methylurea, which was used without further purification. LRMS (M+H⁺) m/z 490.1.

To a solution of the above crude 1-((S)-1-(tert-butyldimethylsilyloxy)-3-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)propan-2-yl)-3-(2-chloro-3-fluorobenzyl)-1-methylurea in THF (300 mL) was added tetrabutylammonium fluoride (10.0 mL, 1 M in THF, 10.0 mmol). The resulting solution was then stirred at RT for 1 h. The reaction mixture was added into a saturated aqueous solution of NH₄Cl (350 mL) and extracted with EtOAc (2×350 mL). Combined organic layers were washed with Brine (2×400 mL) and dried over MgSO₄. The solution was then concentrated. The resulting residue was purified on a silica gel column using a mixture of DCM and MeOH to give 3-(2-chloro-3-fluorobenzyl)-1-(S)-1-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-hydroxypropan-2-yl)-1-methylurea (2.3 g, 61% over two steps). LRMS (M+H⁺) m/z 375.1.

Method B

To a solution of (S)-2-(tert-butoxycarbonylamino) pent-4-enoic acid (20 g, 93 mmol) in anhydrous THF (3 mL) was added LiAlH₄ (2M in THF, 186 mmol). The mixture was heated to 65° C. The reaction was allowed to stir for 3 h until complete by LC/MS. The reaction was cooled to 0° C., and H₂O (7.6 mL) was added and stirred for 4 min, followed by NaOH (3N, 7.6 mL), and a second portion of H₂O (23 mL). The white precipitate was removed by filtration (EtOAc wash) and the filtrate was concentrated to give (S)-2-(methylamino)pent-4-en-1-ol as a clear viscous oil, which was used without further purification.

To a solution of crude (S)-2-(methylamino)pent-4-en-1-ol (˜93 mmol) and DIEA (17.8 mL) in THF (310 mL) was stirred at ambient temperature and the nitrophenol carbamate (18.8 g, 93 mmol) was added in one portion, followed by additional DIEA (32.4 mL). The reaction was stirred for 40 min until deemed complete by LC/MS and diluted with EtOAc (200 mL), washed with saturated Na₂CO₃ (3×50 mL), dried over anhydrous Na₂SO₄ and concentrated. The residue was subjected to flash chromatography (0 to 100% EtOAc in hexanes) to give (S)-3-(2-chloro-3-fluorobenzyl)-1-(1-hydroxypent-4-en-2-yl)-1-methylurea (16.9 g, 52% over 2 steps) as a white solid. LRMS (M+H⁺) m/z 301.0.

A dry 500 mL round-bottom flask was charged with a solution of K₂CO₃ (8.5 g) in water (100 mL). tert-Butanol (100 mL) was added, followed by K₂OsO₂(OH)₄(136 mg, 0.02 equiv.), (DHQD)₂Pyr (363 mg, 0.02 equiv.), and K₃Fe(CN)₆ (20.3 g, 3 equiv.). The mixture was stirred at ambient temperature until most of the solids had dissolved (˜30 min.). The mixture was cooled to 0° C. and the substrate was added (6.2 g, 1 equiv) as a single portion. The reaction was stirred at 4° C. for 24 h. The mixture was allowed to warm to RT, and diluted with water (300 mL). The organic layer was extracted with EtOAc (3×200 mL), dried over anhydrous Na₂SO₄ and concentrated. The resulting crude material was dissolved in acetone (100 mL) and PTSA (400 mg) was added. The reaction was allowed to stir for 3 h, and diluted with EtOAc (100 mL) solid Na₂CO₃ (5 g) was added, and the mixture was stirred for 1 hr. The mixture was filtered and concentrated. The residue was subjected to flash chromatography (0 to 100% EtOAc in hexanes) to give a mixture of diastereomers, which was recrystallized in BuOAc to give 3-(2-chloro-3-fluorobenzyl)-1-(S)-1-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-hydroxypropan-2-yl)-1-methylurea (1.3 g, 17%) as a white solid. LRMS (M+H) m/z 375.1

Example 41 Preparation of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-3-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)propyl isoquinolin-3-ylcarbamate

Method A

To a solution of 1-((S)-1-(tert-butyldimethylsilyloxy)-3-(R)-2,2-dimethyl-1,3-dioxolan-4-yl)propan-2-yl)-3-(2-chloro-3-fluorobenzyl)-1-methylurea (11.4 g, 23 mmol) in THF at 0° C., was added TBAF (23 mmol, 1 equiv.) dropwise. The reaction was completed in 30 min. The solvents were removed. The residue was dissolved in EtOAc (150 mL) and washed with 3% citric acid (150 mL) twice, followed by saturated NaHCO₃ (100 mL) and brine (100 mL). The organic layer was concentrated to give 3-(2-chloro-3-fluorobenzyl)-1-((S)-1-(R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-hydroxypropan-2-yl)-1-methylurea, which was used without further purification. LRMS (M+H⁺) m/z 375.4.

To a mixture of 3-(2-chloro-3-fluorobenzyl)-1-(S)-1-(R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-hydroxypropan-2-yl)-1-methylurea (8.4 g, 22 mmol) in toluene (200 mL) at 100° C. was added acyl azide (4.35 g, 22 mmol, 1 equiv.) in portions. The mixture was stirred at 100° C. for 30 min and concentrated to dryness. The residue was purified on silica gel using a mixture of EtOAc and hexanes to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-3-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)propyl isoquinolin-3-ylcarbamate (7.6 g, 64%) as a light yellow solid. LRMS (M+H⁺) m/z 545.1.

Method B

A 500 mL 3-neck RBF was equipped with magnetic stirrer, heating mantle, set-point controller, thermowell, thermocouple and nitrogen bubbler. The flask was charged with 3-(2-chloro-3-fluorobenzyl)-1-(S)-1-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-hydroxypropan-2-yl)-1-methylurea (15.7 g, 41.9 mmol), iodobenzene diacetate (27 g, 2.0 equiv.) and methyl tert-butyl ether (141 mL). The mixture was warmed to ˜55° C. and the amide (7.6 g, 1.05 equiv.) was added in small portions. The reaction was stirred for 1 h. The reaction was cooled to ambient temperature and quenched by addition of saturated aq. NaHCO₃ (150 mL). The organic phase was extracted with ethyl acetate, and the combined organics were washed with water and brine. The organic phase was dried over MgSO₄ and concentrated. Residual solvents were removed by azeotrope from DCM and hexanes (3×) to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-3-(R)-2,2-dimethyl-1,3-dioxolan-4-yl)propyl isoquinolin-3-ylcarbamate as a solid (25.3 g), which was used without further purification. LRMS (M+H⁺) m/z 545.1.

Example 42 Preparation of sodium (2R,4S)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-2-hydroxy-5-(isoquinolin-3-ylcarbamoyloxy)pentyl phosphate and potassium (2R,4S)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-2-hydroxy-5-(isoquinolin-3-ylcarbamoyloxy)pentyl phosphate

To a solution of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-3-(R)-2,2-dimethyl-1,3-dioxolan-4-yl)propyl isoquinolin-3-ylcarbamate (7.6 g, 14 mmol) in MeOH (35 mL) at 0° C., was added HCl/dioxane (4 N, 35 mL) dropwise. The solution was warmed up to RT and stirred for 2 h. The solvents were removed. DCM (100 mL) was then added. The pH was adjusted by Et₃N to pH 8. The precipitate was filtered and washed with DCM. 6.1 g of desired product was obtained as a white solid. The filtrate was concentrated and purified by HPLC to give 0.4 g of desired product. Combination of products afforded (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate (6.5 g, 92%). LRMS (M+H⁺) m/z 505.1.

To a solution of (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate (2.5 g, 5 mmol) in anhydrous pyridine (20 mL) at −20° C. was added di-tert-butylphosphoryl bromide (5.46 g, 20 mmol, 4 equiv.) dropwise under N₂. The reaction was completed in 5 min. EtOH (1 mL) was added to quench the reaction. The solvents were removed. The residue was dissolved into EtOAc. The pyridine HBr salt was filtered off and the filtrate was concentrated to give (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(di-tert-butoxyphosphoryloxy)-4-hydroxypentyl isoquinolin-3-ylcarbamate, which was used without further purification. LRMS (M+H⁺) m/z 697.2.

To a solution of the above crude (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(di-tert-butoxyphosphoryloxy)-4-hydroxypentyl isoquinolin-3-ylcarbamate in MeOH (8 mL) at 0° C. was added conc. HCl (12 N, 8 mL, 20 equiv.) dropwise. The mixture was stirred for 30 min and concentrated. The residue was dissolved in 50 mL H2O. Aqueous NaOH solution (1 N) was added to adjusted the PH to 3˜4. EtOAc (50 mL) was then added. The mixture was stirred at RT for 1 h. The white solid was then filtered and washed with H₂O and EtOAc, followed by drying in vacuo to give (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4-hydroxy-5-(phosphonooxy)pentyl isoquinolin-3-ylcarbamate as a white powder (2.4 g, 86% for 2 steps). LRMS (M+H) m/z 585.5.

To a solution of (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4-hydroxy-5-(phosphonooxy)pentyl isoquinolin-3-ylcarbamate in MeOH (50 mL) at 0° C. was added NaOH solution (0.5 N, 16 mL, 2 equiv.) dropwise. The solution was stirred at 0° C. for 1 h and concentrated to give sodium (2R,4S)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-2-hydroxy-5-(isoquinolin-3-ylcarbamoyloxy)pentyl phosphate as a white solid (quant.). The solid could be further crystallized by trituration with EtOH, followed by re-crystallization from EtOH—H₂O (6:1) to give the crystalline form. LRMS (M−2Na+3H⁺) m/z 585.5.

To a solution of the above phosphonic acid (2.0 g, 3.4 mmol) in MeOH (20 mL) at 0° C. was added KOH solution (0.5 N, 13.6 mL, 2 equiv.) dropwise. The solution was stirred for 1 h. The solvents were removed. The residue was triturated with EtOH, followed by re-crystallization from EtOH—H₂O (6:1) at 60° C. to give potassium (2R,4S)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-2-hydroxy-5-(isoquinolin-3-ylcarbamoyloxy)pentyl phosphate as a crystalline form. LRMS (M−2K+3H⁺) m/z 585.5.

Example 43 Preparation of sodium (2R,4S)-4-(3-(2,3-difluorobenzyl)-1-methylureido)-2-hydroxy-5-(isoquinolin-3-ylcarbamoyloxy)pentyl phosphate

To a solution of (2S,4R)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl isoquinolin-3-ylcarbamate (4.7 g, 9.62 mmol) in anhydrous pyridine (12 mL) and dichloromethane (36 mL) at −30° C. was added di-tert-butylphosphoryl bromide (7.88 g, 28.87 mmol) dropwise under atmosphere of N₂. The reaction mixture was stirred vigorously at −30° C. for 75 min until the reaction completed. EtOH (2 mL) was then added to quench the reaction. The solvents were removed. The residue was triturated with EtOAc (200 mL). The pyridine HBr salt was filtered off and the filtrate was concentrated to give (2S,4R)-5-(di-tert-butoxyphosphoryloxy)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-4-hydroxypentyl isoquinolin-3-ylcarbamate, which was used without further purification.

To a solution of the crude (2S,4R)-5-(di-tert-butoxyphosphoryloxy)-2-(3-(2,3-difluorobenzyl)-1-methylureido)-4-hydroxypentyl isoquinolin-3-ylcarbamate in MeOH (15 mL) at 0° C. was added conc. HCl (12 N, 16 mL, 192.4 mmol) dropwise. The mixture was stirred for 30 min and concentrated. The residue was dissolved in 50 mL H2O. Aqueous NaOH solution (1 N) was added to adjusted the PH to 3˜4. EtOAc (50 mL) was then added. The mixture was stirred at RT for 1 h. The white solid was then filtered and washed with H₂O and EtOAc and dried under high vacuum to give (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4-hydroxy-5-(phosphonooxy)pentyl isoquinolin-3-ylcarbamate (2.85 g) as a white powder (4.95 g, 89% for 2 steps). LRMS (M−H⁺) m/z 567.5

To a solution of the crude (2.85 g) (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4-hydroxy-5-(phosphonooxy)pentyl isoquinolin-3-ylcarbamate in MeOH (10 mL) at 0° C. was added NaOH solution (0.5 N, 20.07 mL, 2 equiv.) dropwise. The solution was stirred at 0° C. for 1 h and concentrated to give sodium (2R,4S)-4-(3-(2,3-difluorobenzyl)-1-methylureido)-2-hydroxy-5-(isoquinolin-3-ylcarbamoyloxy)pentyl phosphate as a white solid (3.08 g, quant.). LRMS (M−H⁺) m/z 567.5. The solid could be further crystallized by trituration with EtOH, followed by re-crystallization from EtOH—H₂O (6:1) to give the crystalline form.

Example 44 Preparation of (S)-2-(2-chloro-3-fluorobenzyl)(methyl)amino)-3-(2,2-difluoroethylamino)propyl isoquinolin-3-ylcarbamate

To a solution of (S)-tert-butyl 1-(benzyloxy)-3-hydroxypropan-2-ylcarbamate (1.89 g, 6.4 mmol) in DCM (50 mL) was added MsCl (0.55 mL, 7.04 mmol) followed by DIEA (1.27 mL, 7.68 mmol). The mixture was stirred at RT for 30 min and diluted with DCM (300 mL). The organic mixture washed with NaHCO₃, brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The residue was then dissolved in DMF (20.0 mL). To the resulting solution was added NaN₃ (1.25 g, 19.2 mmol) and the mixture was heated at 80° C. for 6 h. LCMS indicated the completion of the reaction. The mixture was cooled to RT and added water (20 mL) and EtOAc (200 mL). The organic layer was separated, washed with NaHCO₃ and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-tert-butyl 1-azido-3-(benzyloxy)propan-2-ylcarbamate (1.5 g, 73% for 2 steps).

To a solution NaH (0.29 g, 7.35 mmol) in DMF (10 mL) was added a solution of (S)-tert-butyl 1-azido-3-(benzyloxy)propan-2-ylcarbamate (1.5 g, 4.9 mmol) in DMF (10.0 mL). The mixture was stirred at RT for 30 min followed by addition of MeI (1.0 mL, 9.8 mmol). The resulting mixture was stirred for another 2 h. LCMS indicated the completion of the reaction. The mixture was quenched with saturated NH₄Cl solution and extracted with EtOAc (200 mL×2). The combined organic layers were washed with brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure to give (S)-tert-butyl 1-azido-3-(benzyloxy)propan-2-yl(methyl)carbamate (1.8 g, crude), which was used without purification.

To a solution of the crude (S)-tert-butyl 1-azido-3-(benzyloxy)propan-2-yl(methyl)carbamate (1.8 g, ˜4.90 mmol) in MeOH (20 mL) was added Pd/C (300 mg). The mixture was transferred to an autoclave reactor, charged with hydrogen (45 psi), and stirred at RT overnight. The solid was filtered off. To the filtrate were added CbzCl (0.83 mL, 5.88 mmol) and DIEA (1.22 mL, 7.35 mmol) and the resulting mixture was stirred at RT for 30 min. The reaction mixture was concentrated under reduced pressure and dissolved in EtOAc. The organic mixture was washed with NaHCO₃ and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure to give [(S)-2-(tert-Butoxycarbonyl-methyl-amino)-3-hydroxy-propyl]carbamic acid benzyl ester (2.2 g of crude), which was used without purification (2.2 g, crude). LRMS (M+H⁺-Boc) m/z 239.1.

To a solution of [(S)-2-(tert-Butoxycarbonyl-methyl-amino)-3-hydroxy-propyl]carbamic acid benzyl ester (2.2 g of crude mixture, 4.90 mmol) in toluene (20 mL) was added isoquinoline-3-carbonyl azide (1.16 g, 5.39 mmol) in portions and the mixture was heated to 100° C. for 1 h. The mixture was concentrated to one forth of the amount and the remaining residue was purified on silica gel column using a mixture of EtOAc and hexanes to give [(S)-2-(tert-Butoxycarbonyl-methyl-amino)-3-(isoquinolin-3-ylcarbamoyloxy)-propyl]-carbamic acid benzyl ester (1.5 g, 58% for 4 steps). LRMS (M+H⁺) m/z 527.3.

To a solution of [(S)-2-(tert-Butoxycarbonyl-methyl-amino)-3-(isoquinolin-3-ylcarbamoyloxy)-propyl]-carbamic acid benzyl ester (4.58 g, 9.0 mmol) in MeOH (7.5 mL) was added HCl (4 N in 1,4-dioxane, 22.5 mL, 90.0 mmol). The mixture was stirred at RT for 2 h, concentrated, and re-dissolved in EtOAc. The organic mixture was washed with sat. NaHCO₃, water, and brine, dried over Na₂SO₄, filtered, and concentrated to give Isoquinolin-3-yl-carbamic acid (S)-3-benzyloxycarbonylamino-2-methylamino-propyl ester (3.59 g), which was used without further purification. LRMS (M+H⁺) m/z 409.2.

To a solution of the crude isoquinolin-3-yl-carbamic acid (S)-3-benzyloxycarbonylamino-2-methylamino-propyl ester (9.0 mmol) in THF (35 mL) were added 4-nitrophenyl 2-chloro-3-fluorobenzylcarbamate (2.85 g, 8.79 mmol) and DIEA (2.3 mL, 13.2 mmol) at RT. The reaction mixture was stirred at RT for 30 min. The solvent was removed and the residue was dissolved in EtOAc (400 mL). The organic mixture was washed with NaOH (1 N, 50 mL×3), HCl (0.5 N, 50 mL), saturated NaHCO₃, and brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The residue was purified on silica gel column using a mixture of EtOAC and hexanes to give Isoquinolin-3-yl-carbamic acid (S)-3-benzyloxycarbonylamino-2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-propyl ester (3.8 g, 71% for two steps) as white foam. LRMS (M+H⁺) m/z 594.2.

To a solution of isoquinolin-3-yl-carbamic acid (S)-3-benzyloxycarbonylamino-2-[3-(2-chloro-3-fluoro-benzyl)-1-methyl-ureido]-propyl ester (1.3 g, 2.13 mmol) in CH₃CN (20.0 mL) was added TMSI (0.35 mL, 2.56 mmol). The mixture was stirred at RT for 15 min and quenched with MeOH (20.0 mL). The resulting mixture was stirred for another 15 min, concentrated to dryness, and partitioned in between ether (30 mL) and HCl (2 N, 20 mL). The aqueous layer was separated, basified to pH 9, and extracted with EtOAc (200 mL×2). The combined organic layers were washed brine, dried over Na₂SO₄, filtered, and concentrated under reduced pressure to give (S)-3-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)propyl isoquinolin-3-ylcarbamate (2.7 g) as a light yellow foam solid, which was used without further purification. LRMS (M+H⁺) m/z 460.1.

To a solution of (S)-3-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)propyl isoquinolin-3-ylcarbamate (200 mg, 0.44 mmol) in THF (2.0 mL) were added 2,2-difluoroethyl trifluoromethanesulfonate (94 mg, 0.44 mmol) and DIEA (0.15 mL, 0.88 mmol) at RT The reaction mixture was stirred at RT for 30 min. The solvent was removed. The resulting residue was dissolved in MeOH and mixture was purified on RP-HPLC using a mixture of acetonitrile and water to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-3-(2,2-difluoroethylamino)propyl isoquinolin-3-ylcarbamate (130 mg, 56% for two steps). LRMS (M+H⁺) m/z 524.2.

Example 45 Preparation of (S)-2-((2-chloro-3-fluorobenzyl)(methyl)amino)-3-(2,2-difluoroethylamino)propyl 3-(3-fluorophenyl)isoxazol-5-ylcarbamate

To a solution of (S)-tert-butyl 1-azido-3-(benzyloxy)propan-2-yl(methyl)carbamate (4 g, 11.66 mmol) in EtOH (100 mL) and AcOH (10 mL) was added Pd/C (10%, 1.0 g). The resulting mixture was transferred to an autoclave and charged with hydrogen (45 psi). The reaction mixture was stirred at RT for 1 h and filtered. The filtrate was concentrated to give (S)-tert-butyl 1-amino-3-(benzyloxy)propan-2-yl(methyl)carbamate, which was used without further purification. LRMS (M+Na⁺) m/z 317.2.

To a solution of (S)-tert-butyl 1-amino-3-(benzyloxy)propan-2-yl(methyl)carbamate (5.1 mmol) in MeOH (50 mL) were added 2,2-difluoroethyl trifluoromethanesulfonate (1.09 g, 5.1 mmol) and DIEA (1.68 mL, 10.2 mmol). The resulting mixture was stirred at RT for 1 h followed by addition of Boc₂O (1.67 g, 7.65 mmol). The mixture was concentrated and the residue was purified on silica gel column using a mixture of EtOAc and hexanes to give [(S)-3-Benzyloxy-2-(tert-butoxycarbonyl-methyl-amino)-propyl]-(2,2-difluoro-ethyl)-carbamic acid tert-butyl ester (2.42 g, quant.). LRMS (M+Na⁺) m/z 481.2.

To a solution of [(S)-3-Benzyloxy-2-(tert-butoxycarbonyl-methyl-amino)-propyl]-(2,2-difluoro-ethyl)-carbamic acid tert-butyl ester (2.42 g, 5.28 mmol) in MeOH (20 mL) and AcOH (2.0 mL) was added Pd/C (10%, 1.0 g). The reaction mixture was transferred to an autoclave and charged with hydrogen (50 psi). The mixture was stirred RT for 20 h and filtered. The filtrated was concentrated and the residue was purified on silica gel using a mixture of EtOAc and hexanes to give [(S)-2-(tert-Butoxycarbonyl-methyl-amino)-3-hydroxy-propyl]-(2,2-difluoro-ethyl)-carbamic acid tert-butylester (1.81 g, 93%). LRMS (M+Na⁺) m/z 391.2.

To a solution of [(S)-2-(tert-Butoxycarbonyl-methyl-amino)-3-hydroxy-propyl]-(2,2-difluoro-ethyl)-carbamic acid tert-butylester (200 mg, 0.86 mmol) in toluene (8.0 mL) was added 3-(3-fluorophenyl)isoxazole-5-carbonyl azide (317 mg, 0.86 mmol). The resulting solution was stirred at 100° C. for 1 h. The mixture was cooled and concentrated. The residue was purified on RP-HPLC using a mixture of acetonitrile and water to give {(S)-2-(tert-Butoxycarbonyl-methyl-amino)-3-[3-(3-fluoro-phenyl)-isoxazol-5-ylcarbamoyloxy]-propyl}-(2,2-difluoro-ethyl)-carbamic acid tert-butyl ester (291 mg, 60%). LRMS (M+Na⁺) m/z 595.2.

To a solution of {(S)-2-(tert-Butoxycarbonyl-methyl-amino)-3-[3-(3-fluoro-phenyl)-isoxazol-5-ylcarbamoyloxy]-propyl}-(2,2-difluoro-ethyl)-carbamic acid tert-butyl ester (291 mg, 0.62 mmol) in DCM (5 mL) was added TFA (1.0 mL). The mixture was stirred at RT for 1 h, concentrated, and dissolved in THF (10 mL). To the resulting solution were added 4-nitrophenyl 2-chloro-3-fluorobenzylcarbamate (220 mg, 0.68 mmol) and TEA (0.3 mL, 1.24 mmol) at 0° C. The resulting mixture was stirred at 0° C. for 1 h. The solvent was removed and the resulting residue was purified on RP-HPLC using a mixture of acetonitrile and water to give (S)-2-(2,3-difluorobenzyl)(methyl)amino)-5-(2-methyl-6,7-dihydro-1H-imidazo[4,5-c]pyridin-5(4H)-yl)-5-oxopentyl isoquinolin-3-ylcarbamate (135 mg, 39% for two steps) as white solid. LRMS (M+H⁺) m/z 559.2.

Example 46 Preparation of (S)-2-((2-chloro-3-fluorobenzyl)(methyl)amino)-5-(2-methyl-6,7-dihydro-1H-imidazo[4,5-c]pyridin-5(4H)-yl)-5-oxopentyl isoquinolin-3-ylcarbamate

To a solution of (S)-methyl 4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(isoquinolin-3-ylcarbamoyloxy)pentanoate (220 mg, 0.43 mmol) in 1,4-dioxane (5 mL) was added LiOH (2N, 1.3 mL, 2.6 mmol). The reaction mixture was stirred at RT for 1 h and concentrated to give lithium (S)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(isoquinolin-3-ylcarbamoyloxy)pentanoate, which was used without further purification. LRMS (M+H⁺) m/z 503.2.

To a suspension of lithium (S)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(isoquinolin-3-ylcarbamoyloxy)pentanoate (0.43 mmol) and HBTU (244 mg, 0.64 mmol) in DMF (5 mL) was added 2-methyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine dihydrochloride. The resulting mixture was stirred at RT for 1 h, filtered, and purified on RP-HPLC using a mixture of acetonitrile and water to give (S)-2-((2-chloro-3-fluorobenzyl)(methyl)amino)-5-(2-methyl-6,7-dihydro-1H-imidazo[4,5-c]pyridin-5(4H)-yl)-5-oxopentyl isoquinolin-3-ylcarbamate (182.1 mg, 68% for two steps). LRMS (M+H⁺) m/z 622.2.

Example 47 Preparation of (S)-5-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,4-difluoropentyl 6-fluoroisoquinolin-3-ylcarbamate

To a mixture of S-(+)-5-hydroxymethyl-2-pyrrolidinone (7.5 g, 65.1 mmol) and 2,2-dimethoxypropane (DMP) (50 mL) was added camphorsulfonic acid (CSA) (753 mg, cat.). The mixture was refluxed for 2 h, and concentrated in vacuo. Fresh DMP (50 mL) was then added, and the mixture was refluxed overnight. After concentrated, the remaining residue was purified on pre-silica gel column (hexane and ethyl acetate) to give (S)-3,3-dimethyl-dihydropyrrolo[1,2-c]oxazol-5(1H,3H,6H)-one as a pale yellow oil (4.0 g, 40%). LRMS (M+H⁺) m/z 156.2.

To a mixture of diisopropylamine (58.2 mL, 0.412 mol, 2.0 equiv), and THF (600 mL) at −78° C. was added a solution of ^(n)BuLi (39.1 mL, 0.391 mmol, 1.9 equiv) (10M) slowly, and the resulting solution was stirred for 40 min. A solution of (S)-3,3-dimethyl-dihydropyrrolo[1,2-c]oxazol-5(1H,3H,6H)-one (32 g, 0.206 mmol) in THF (50 mL) was added slowly. The resulting light yellow mixture was stirred at −78° C. for 1 h. After addition of a solution of NFSi (84.4 g, 0.268 mmol, 1.3 equiv) in THF (100 mL), the reaction was allowed to stir below −55° C. for 1 h. The reaction was quenched with saturated aqueous NH₄Cl, and the mixture was warmed to RT The THF was removed in vacuo, and the resulting residue was partitioned between EtOAc and H₂O. After separating layers, the aqueous layer was extracted further with EtOAc. The combined organic layers were dried (Na₂SO₄), filtered, and concentrated to leave an orange residue that was purified by silica gel column (hexanes/EtOAc) to give (S)-6,6-difluoro-3,3-dimethyl-dihydropyrrolo[1,2-c]oxazol-5(1H,3H,6H)-one and (5S)-2,2-(7aS)-6-fluoro-3,3-dimethyl-dihydropyrrolo[1,2-c]oxazol-5(1H,3H,6H)-one as an oil-like solid (20.0 g, 55.8%). LRMS (M+H⁺) m/z 174.2.

(5S)-2,2-(7aS)-6-fluoro-3,3-dimethyl-dihydropyrrolo[1,2-c]oxazol-5(1H,3H,6H)-one (20.0 g, 0.115 mol) was subjected to the same fluorination procedure second time to give ((S)-6,6-difluoro-3,3-dimethyl-dihydropyrrolo[1,2-c]oxazol-5(1H,3H,6H)-one (15.0 g, 68.2%) LRMS (M+H⁺) m/z 192.2.

To a solution of (S)-6,6-difluoro-3,3-dimethyl-dihydropyrrolo[1,2-c]oxazol-5(1H,3H,6H)-one (1.35 g, 0.706 mmol) in methanol (10 mL) was added HCl in dioxane (2.65 mL, 4N) under ice-water bath and then stirred at RT overnight. The reaction mixture was concentrated. The resulting residue was dissolved in THF (10 mL) and TEA (5 mL) was added. The resulting solution was stirred for 1 h. The reaction mixture was concentrated to give a crude mixture. Purification by flash column chromatography (hexanes/EtOAc) gave (S)-3,3-difluoro-5-(hydroxymethyl)pyrrolidin-2-one (0.80 g 75%). LRMS (M+H⁺)m/z 152.2.

To a mixture of (S)-3,3-difluoro-5-(hydroxymethyl)pyrrolidin-2-one (28.9 g, 0.191 mol), triethyl amine (53.2 mL, 0.382 mol) and DMAP (11.7 g, 0.0955 mol) in THF (200 mL) was added Di-t-butyl-dicarbonate (83.4 g, 0.382 mol). The reaction mixture was stirred for 2 h and concentrated. The resulting residue was diluted with methanol (200 mL) and potassium cyanide (3.6 g, 0.0955 mol) was added. The resulting mixture was stirred for 1 h. The solvents were removed in vacuo, and the resulting residue was partitioned between DCM and H₂O. After separating layers, the aqueous layer was extracted further with DCM. The combined organic layers were dried (Na₂SO₄), filtered, and concentrated, and the resulting residue was purified by silica gel column (hexanes/EtOAc) to give (S)-methyl 4-(tert-butoxycarbonylamino)-5-(tert-butoxycarbonyloxy)-2,2-difluoropentanoate (44.1 g, 60%). LRMS (M+Na⁺) m/z 406.4

To a mixture of (S)-methyl 4-(tert-butoxycarbonylamino)-5-(tert-butoxycarbonyloxy)-2,2-difluoropentanoate (46.0 g, 0.12 mol) and MeI (15.0 mL, 0.24 mol) in DMF (300 mL) was added sodium hydride (60%, 7.2 g, 0.18 mol) at 0° C. The reaction mixture was stirred at 0° C. for 3 h and LC-MS showed the reaction was completed. The reaction was quenched with saturated NH₄Cl solution and filtered. The filtrate was concentrated to remove most of DMF and the residue was dissolved in EtOAc (1.5 L). The organic layer was washed with water and brine, dried over Na₂SO₄. The organic layers were combined and concentrated. The resulting residue was purified on silica gel column (hexanes/EtOAc) to give (S)-methyl 4-(tert-butoxycarbonyl(methyl)amino)-5-(tert-butoxycarbonyloxy)-2,2-difluoropentanoate (42 g, 88%). LRMS (M+Na⁺) m/z 420.4.

To a solution of (S)-methyl 4-(tert-butoxycarbonyl(methyl)amino)-5-(tert-butoxycarbonyloxy)-2,2-difluoropentanoate (42.0 g, 0.106 mol) in THF (300 mL) was added Lithium borohydride (79.3 mL, 2 M, 0.159 mol) in THF at 0° C. The reaction mixture was stirred at 0° C. for 1 h and at RT for 2 h. LC-MS showed the reaction was complete. The reaction mixture was concentrated and partitioned between EtOAc and H₂O. After separating layers, the aqueous layer was extracted further with EtOAc. The combined organic layers were dried (Na₂SO₄), filtered, and concentrated, and the resulting residue was purified by silica gel column (hexanes/EtOAc) to give (S)-tert-butyl 1-(tert-butoxycarbonyloxy)-4,4-difluoro-5-hydroxypentan-2-yl(methyl)carbamate (35.3 g, 90%). LRMS (M+Na⁺) m/z 392.4.

To a mixture of (S)-tert-butyl 1-(tert-butoxycarbonyloxy)-4,4-difluoro-5-hydroxypentan-2-yl(methyl)carbamate (35.3 g, 0.0956 mol) and lutidine (22.2 mL, 0.191 mol) in DCM (300 mL) was added trifluoromethanesulfonic anhydride (19.3 mL, 0.115 mol) at 0° C. The reaction mixture was stirred at 0° C. for 1 h. LC-MS showed the reaction was complete. The reaction mixture was concentrated down. The resulting residue was dissolved in DMF (100 mL) and sodium azide (62.1 g, 0.956 mol) was added. The reaction mixture was stirred at RT overnight. The reaction solution was partitioned between EtOAc and saturated sodium bicarbonate solution. After separating layers, the aqueous layer was extracted further with EtOAc. The combined organic layers were dried (Na₂SO₄), filtered, and concentrated, and the resulting residue was purified by silica gel column (hexanes/EtOAc) to give (S)-tert-butyl 5-azido-1-(tert-butoxycarbonyloxy)-4,4-difluoropentan-2-yl(methyl)carbamate (0.0956 mol, 100%). LRMS (M+Na⁺) m/z 417.4.

To a solution of (S)-tert-butyl 5-azido-1-(tert-butoxycarbonyloxy)-4,4-difluoropentan-2-yl(methyl)carbamate (95.6 mmol) in methanol (10 mL) was added Hydrogen chloride (4.0 M in 1,4-dioxane, 240 mL, 0.596 mol). The resulting solution was stirred for overnight. The solvent was removed, and the remaining residue was dried under reduced pressure to give (S)-5-azido-4,4-difluoro-2-(methylamino)pentan-1-ol as a HCl salt, which was used without further purification. LRMS (M+H⁺) m/z 195.3.

To a solution of (S)-5-azido-4,4-difluoro-2-(methylamino)pentan-1-ol HCl salt (95.6 mmol) and DIEA (33.3 mL, 0.191 mol) in THF (300 mL) was added O-(4-nitrophenyl)-N-(2-chloro-3-fluorobenzyl) carbamate (34.1 g, 0.105 mol). The resulting mixture was stirred at RT for 1 h. The solvent was removed, and the resulting residue was purified on silica gel column (DCM/MeOH) to give (S)-1-(5-azido-4,4-difluoro-1-hydroxypentan-2-yl)-3-(2-chloro-3-fluorobenzyl)-1-methylurea (25.4 g, 70%). LRMS (M+H⁺) m/z 380.4.

To a solution of (S)-1-(5-azido-4,4-difluoro-1-hydroxypentan-2-yl)-3-(2-chloro-3-fluorobenzyl)-1-methylurea (25.4 g, 0.0669 mol) and toluene (500 mL) was added 6-fluoroisoquinoline-3-carbonyl azide (17.4 g, 0.0803 mol). The resulting solution was stirred at 100 C for 2 h and concentrated, and the remaining residue was purified on silica gel column (DCM/MeOH) to give (S)-5-azido-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,4-difluoropentyl 6-fluoroisoquinolin-3-ylcarbamate (25.0 g, 84.7%). LRMS (M+H⁺) m/z 568.5.

To a mixture of (S)-5-azido-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,4-difluoropentyl 6-fluoroisoquinolin-3-ylcarbamate (25.0 g, 0.0441 mol), THF (300 mL) and water (100 mL) was added triphenylphosphine (13.9 g, 0.0529 mol) and aq. HCl solution (53 mL, 2N, 0.106 mol). The resulting mixture was stirred at RT for 1 h and concentrated down to about 200 mL. Water (200 mL) was then added. The resulting mixture (pH<4) was extracted with EtOAc (300 mL) and the EtOAc solution was discarded. The remaining aq. solution was adjusted to pH>8 by adding NaOH (2N) and extracted with DCM (200 mL×3). The organic layer was washed with water and brine, dried over Na₂SO₄. The organic layers were combined and concentrated. The resulting residue was purified on silica gel column (DCM/MeOH) to give (S)-5-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,4-difluoropentyl 6-fluoroisoquinolin-3-ylcarbamate (12.1 g, 50.7%). LRMS (M+H⁺) m/z 542.5.

Example 48 Preparation of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-3-(5,6,7,8-tetrahydroimidazo[1,5-a]pyrazin-3-yl)propyl isoquinolin-3-ylcarbamate

To a mixture of (S)-2-((benzyloxycarbonyl)(methyl)amino)-4-tert-butoxy-4-oxobutanoic acid dicyclohexylamimonium salt (20 g, 0.0386 mol) and Et₃N (7.90 mL, 0.0579 mol) in THF (500 mL) was added isobutyl chloroformate (6.05 mL, 0.0463 mol) at 0° C. The reaction mixture was stirred for 1 h, and filtered to remove TEA salt. To the filtrate was added a solution of NaBH₄ (2.19 g, 0.0579 mol) in THF (50 mL) and water (100 mL) at 0-5° C. The reaction mixture was stirred at RT for 1 h and quenched with saturated NH₄Cl solution. The reaction mixture was concentrated to remove most of THF and extracted with EtOAc (700 mL×3). The organic layers were washed with water, NaHCO3 and brine, dried over Na₂SO₄, and concentrated to give (S)-tert-butyl 3-((benzyloxycarbonyl)(methyl)amino)-4-hydroxybutanoate (10 g), which was used without further purification. LRMS (M+Na⁺) m/z 346.1.

To a mixture of (S)-tert-butyl 3-((benzyloxycarbonyl)(methyl)amino)-4-hydroxybutanoate (4.0 g, 12.4 mmol) and toluene (100 mL) was added isoquinoline-3-carbonyl azide (2.94 g, 14.9 mmol). The resulting mixture was stirred at 100° C. for 2 h. The solvent was removed, and the remaining residue was purified on silica gel column (hexanes/EtOAc) to give (S)-tert-butyl 3-((benzyloxycarbonyl)(methyl)amino)-4-(isoquinolin-3-ylcarbamoyloxy)butanoate (3.6 g, 58.9%). LRMS (M+H⁺) m/z 494.1.

To a solution of (S)-tert-butyl 3-((benzyloxycarbonyl)(methyl)amino)-4-(isoquinolin-3-ylcarbamoyloxy)butanoate (1.8 g, 3.65 mmol) and MeOH (5 mL) was added 10% Pd—C (500 mg). The resulting mixture was stirred under 12 psi of hydrogen for 1 h. The mixture was filtered and concentrated, and the remaining residue was dried in vacuo to give (S)-tert-butyl 4-(isoquinolin-3-ylcarbamoyloxy)-3-(methylamino)butanoate (1.3 g), which was used without further purification. LRMS (M+H⁺) m/z 360.1

To a mixture of (S)-tert-butyl 4-(isoquinolin-3-ylcarbamoyloxy)-3-(methylamino)butanoate (1.3 g, 3.65 mmol) and DIEA (1.27 mL, 7.3 mmol) in THF (50 mL) was added O-(4-nitrophenyl)-N-(2-chloro-3-fluorobenzyl) carbamate (1.78 g, 0.00547 mol). The resulting mixture was stirred at RT for 2 h and diluted with EtOAc (100 mL). The organic layer was washed by NaHCO₃ solution and concentrated. The resulting residue was purified on silica gel column (hexanes/EtOAc) to give (S)-tert-butyl 3-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4-(isoquinolin-3-ylcarbamoyloxy)butanoate (1.1 g, 55.3%). LRMS (M+H⁺) m/z 545.1.

To a mixture of (S)-tert-butyl 3-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4-(isoquinolin-3-ylcarbamoyloxy)butanoate (0.8 g, 1.47 mmol) and DCM (10 mL) was added TFA (10 mL). The resulting solution was stirred at RT for 1 h. The mixture was concentrated, and the remaining residue was dried in vacuo to give (S)-3-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4-(isoquinolin-3-ylcarbamoyloxy)butanoic acid (1.3 g), which was used without further purification. LRMS (M+H⁺) m/z 489.1.

To a mixture of the crude (S)-3-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4-(isoquinolin-3-ylcarbamoyloxy)butanoic acid (1.47 mmol) and DMF (5 mL) were added DIEA (0.512 mL, 2.94 mmol) and HBTU (0.667 g, 1.76 m mol). The resulting mixture was stirred at RT for 10 min and 2-aminomethylpyrazine (0.192 g, 1.76 mmol) was added. The resulting mixture was stirred at RT for 30 min. The mixture was diluted with EtOAc (100 mL). The organic layer was washed by NaHCO₃ solution and concentrated. The resulting residue was purified on silica gel column (DCM/MeOH) to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4-oxo-4-(pyrazin-2-ylmethylamino)butyl isoquinolin-3-ylcarbamate (0.65 g, 76.2%). LRMS (M+H⁺) m/z 580.1

To a mixture of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4-oxo-4-(pyrazin-2-ylmethylamino)butyl isoquinolin-3-ylcarbamate (650 mg, 1.12 mmol) and DCM (50 mL) were added phosphoryl chloride (0.514 mL, 0.00561 mol). The resulting mixture was stirred at RT for overnight. The resulting solution was concentrated. The resulting residue was purified on prep-HPLC (ACN/H₂O with 0.1% HCOOH) to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-3-(imidazo[1,5-a]pyrazin-3-yl)propyl isoquinolin-3-ylcarbamate (0.27 g, 43%). LRMS (M+H⁺) m/z 562.1

To a solution of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-3-(imidazo[1,5-a]pyrazin-3-yl)propyl isoquinolin-3-ylcarbamate (100 mg, 0.178 mmol) and MeOH (5 mL) were added 10% Pd—C (100 mg). The resulting mixture was stirred under 12 psi of hydrogen for h. The mixture was filtered and concentrated. The resulting residue was purified on prep-HPLC (ACN/H2O with 0.1% HCOOH) to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-3-(5,6,7,8-tetrahydroimidazo[1,5-a]pyrazin-3-yl)propyl isoquinolin-3-ylcarbamate (35 mg, 35%). LRMS (M+H⁺) m/z 566.1.

Example 49 Preparation of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(3-(2-hydroxyethyl)ureido)pentyl 6-fluoroisoquinolin-3-ylcarbamate

To a mixture of (S)-5-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentyl 6-fluoroisoquinolin-3-ylcarbamate (0.40 g, 0.792 mmol), DIEA (0.276 mL, 1.58 mmol) and THF (2 mL), ethyl isocyanatoacetate (0.108 mL, 0.950 mmol) was added. The mixture was refluxed for 30 min, and concentrated. The remaining residue was purified on silica gel column (DCM/MeOH) to give (S)-ethyl 1-(2-chloro-3-fluorophenyl)-5-((6-fluoroisoquinolin-3-ylcarbamoyloxy)methyl)-4-methyl-3,10-dioxo-2,4,9,11-tetraazatridecan-13-oate (0.40 g, 80%). LRMS (M+H⁺) m/z 635.6.

To a solution of (S)-ethyl 1-(2-chloro-3-fluorophenyl)-5-(6-fluoroisoquinolin-3-ylcarbamoyloxy)methyl)-4-methyl-3,10-dioxo-2,4,9,11-tetraazatridecan-13-oate (0.40 g, 0.63 mmol) in THF (20 mL) was added Lithium borohydride (1.57 mL, 2 M, 3.15 mmol) in THF at 0° C. The reaction was stirred at 0° C. for 10 min. MeOH (1 mL) was added to the reaction solution and the resulting solution was stirred at RT for 2 h. The reaction was quenched with saturated NH₄Cl solution. The resulting residue was partitioned between EtOAc and H₂O. The aqueous layer was extracted further with EtOAc. The combined organic layers were dried (Na₂SO₄), filtered, and concentrated, and the resulting residue was purified by silica gel column (hexanes/EtOAc) to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(3-(2-hydroxyethyl)ureido)pentyl 6-fluoroisoquinolin-3-ylcarbamate (0.34 g, 91%). LRMS (M+Na⁺) m/z 593.6.

Example 50 Preparation of (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl 3-phenylisoxazol-5-ylcarbamate

To a solution of 3-(2-chloro-3-fluorobenzyl)-1-((S)-1-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-hydroxypropan-2-yl)-1-methylurea (0.52 g, 1.4 mmol, 1.0 equiv.) in toluene (20 mL) at 100° C., was added 3-phenylisoxazole-5-carbonyl azide (0.3 g, 1.4 mmol, 1.0 equiv.). The solution was stirred for 1 h. The solvent was removed, and the remaining residue was purified on silica gel column using a mixture of hexane and EtOAc to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-3-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)propyl 3-phenylisoxazol-5-ylcarbamate (0.42 g, 60%). LRMS (M+H⁺) m/z 561.1.

To a solution of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-3-(R)-2,2-dimethyl-1,3-dioxolan-4-yl)propyl 3-phenylisoxazol-5-ylcarbamate (0.4 g, 0.7 mmol, 1.0 equiv.) in MeOH (5 mL) at 0° C., was added HCl/Dioxane (4 N, 3 mL). The mixture was warmed up to RT, stirred for 1 h, concentrated and purified on silica gel column using a mixture of DCM and MeOH to give (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl 3-phenylisoxazol-5-ylcarbamate (0.35 g, 96%, white solid). LRMS (M+H⁺) m/z 521.1.

Example 51 Preparation of Sodium (2R,4S)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-2-hydroxy-5-(3-phenylisoxazol-5-ylcarbamoyloxy)pentyl phosphate

To a mixture of (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,5-dihydroxypentyl 3-phenylisoxazol-5-ylcarbamate (0.25 g, 0.48 mmol, 1.0 equiv.), DMAP (0.23 g, 1.92 mmol, 4.0 equiv.), and DIEA (0.33 mL, 1.92 mmol, 4.0 equiv.) in DCM (50 mL) at ° C., was added diethyl chlorophorophosphate (0.20 mL, 1.44 mmol, 3.0 equiv.) dropwise. The reaction was quenched with EtOH in 5 min, followed by treatment with saturated NaHCO₃. The organic layer was concentrated, and the resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(diethoxyphosphoryloxy)-4-hydroxypentyl 3-phenylisoxazol-5-ylcarbamate (56 mg, 20%). LRMS (M+H⁺) m/z 657.1.

To a mixture of (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(diethoxyphosphoryloxy)-4-hydroxypentyl 3-phenylisoxazol-5-ylcarbamate (56 mg, 0.085 mmol, 1.0 equiv.) in acetonitrile (5 mL) was added TMSI (0.115 mL, 0.85 mmol, 10.0 equiv.) at ° C. After stirring at RT for 10 min, the reaction wag quenched with MeOH. The solvent was removed, and the resulting residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O (with 0.1% TFA buffer). The fractions of product was concentrated, dissolved in a mixture of methanol and water (2:1), followed by addition of HCl (4 N in 1,4-dioxane, 2 mL). The mixture was concentrated to give (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4-hydroxy-5-(phosphonooxy)pentyl 3-phenylisoxazol-5-ylcarbamate (48 mg, 94%) as a white solid. LRMS (M+H⁺) m/z 601.5.

To a mixture of (2S,4R)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4-hydroxy-5-(phosphonooxy)pentyl 3-phenylisoxazol-5-ylcarbamate (48 mg, 0.08 mmol, 1.0 equiv.) at 0° C., was added NaOH (0.1 N, 1.6 mL, 2.0 equiv.) dropwise. The mixture was stirred at RT for 1 h followed by concentration to give sodium (2R,4S)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-2-hydroxy-5-(3-phenylisoxazol-5-ylcarbamoyloxy)pentyl phosphate (55 mg, quant.) as a white solid. LRMS (M−2Na⁺ 3H⁺) m/z 601.5.

Example 52 Preparation of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-oxo-5-(piperazin-1-yl)pentyl 3-(3-fluorophenyl)isoxazol-5-ylcarbamate

To a mixture of (S)-methyl 4-(tert-butoxycarbonyl(methyl)amino)-5-(tert-butyldimethylsilyloxy)pentanoate (41 g, 109 mmol, 1.0 equiv.), lutidine (19 mL, 163 mmol, 1.5 equiv.) in DCM (400 mL) at 0° C., was added TMSOTf (23.7 mL, 131 mmol, 1.2 equiv.) dropwise. The solution was stirred at RT for 1 h. The solvents were removed and the residue was used without further purification.

To a solution of 4-nitrophenylchloroformate (24.22 g, 120 mmol, 1.1 equiv.) in THF (100 mL) was added a solution of 2-chloro-3-fluorobenzylamine (19.1 g, 120 mmol, 1.1 equiv.) and DIEA (46 mL, 264 mmol, 2.2 equiv.) in THF (100 mL). The resulting solution was stirred at RT for 20 min. The reaction mixture was added into a solution of (S)-methyl 5-(tert-butyldimethylsilyloxy)-4-(methylamino)pentanoate (30 g, 109 mmol, 1.0 equiv.), DIEA (23 mL, 132 mmol, 1.1 equiv.) in THF (100 mL). The resulting mixture was stirred at RT for 1 h. The solvent was removed, and the resulting residue was dissolved into EtOAc (300 mL) and washed with brine (400 mL), saturated Na₂CO₃ (400 mL), and brine (400 mL). The organic layer was concentrated and the residue was purified on silica gel column using a mixture of Hexane and EtOAc to give (S)-methyl 5-(tert-butyldimethylsilyloxy)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentanoate (32.6 g, 65%) as a yellowish solid. LRMS (M+H⁺) m/z 461.1.

To a solution of (S)-methyl 5-(tert-butyldimethylsilyloxy)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentanoate (5.3 g, 11.5 mmol, 1.0 equiv.) in dioxane (60 mL), was added LiOH (1 N, 34.5 mL, 3 equiv.) dropwise. The solution was stirred at RT for 1 h. The solvents were removed and the residue was used without further purification.

To a solution of (S)-5-(tert-butyldimethylsilyloxy)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentanoic acid (4.46 g, 10 mmol, 1.0 equiv.) in DMF (50 mL), was added HBTU (5.69 g, 15 mmol, 1.5 equiv.), 1-N-Boc-piperazine (2.79 g, 15 mmol, 1.5 equiv.) and DIEA (5.21 mL, 30 mmol, 3.0 equiv.) in sequence. The reaction was completed in 15 min. Ether (100 mL) and brine (100 mL) were added to the reaction mixture. The organic layer was dried and concentrated. The residue was purified on silica gel column using a mixture of hexane and EtOAc to give (S)-tert-butyl 4-(5-(tert-butyldimethylsilyloxy)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentanoyl)piperazine-1-carboxylate (4.2 g, 68%). LRMS (M+H⁺) m/z 615.2.

To a solution of (S)-tert-butyl 4-(5-(tert-butyldimethylsilyloxy)-4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)pentanoyl)piperazine-1-carboxylate (4.2 g, 6.8 mmol, 1.0 equiv.) in MeOH (35 mL), was added HCl (2N, 0.68 mL, 1.36 mmol, 0.2 equiv.). The reaction was stirred at RT for 1 h. NaHCO₃ (1.1 g, 13.6 mmol, 2.0 equiv) was added to quench the reaction. The solvents were removed. The residue was dissolved in EtOAc (100 mL). The salt was filtered off and the filtrate was concentrated to give (S)-tert-butyl 4-(4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-hydroxypentanoyl)piperazine-1-carboxylate (3.4 g, quant.). LRMS (M+H⁺) m/z 501.2.

To a solution of (S)-tert-butyl 4-(4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-hydroxypentanoyl)piperazine-1-carboxylate (0.30 g, 0.6 mmol, 1.0 equiv.) in toluene (10 mL) at 100° C., was added 3-(3-fluorophenyl)isoxazole-5-carbonyl azide (0.13 g, 0.6 mmol, 1.0 equiv.). The solution was stirred for 1 h. The solvent was removed and the residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (S)-tert-butyl 4-(4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(3-(3-fluorophenyl)isoxazol-5-ylcarbamoyloxy)pentanoyl)piperazine-1-carboxylate (0.3 g, 60%). LRMS (M+H⁺) m/z 705.1.

To a solution of (S)-tert-butyl 4-(4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(3-(3-fluorophenyl)isoxazol-5-ylcarbamoyloxy)pentanoyl)piperazine-1-carboxylate (0.3 g, 0.36 mmol, 1.0 equiv.) in MeOH (2 mL) at 0° C., was added HCl/dioxane (4 N, 0.9 mL, 3.6 mmol, 10 equiv.). The solution was stirred at RT for 1 h. The solvents were removed and the residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O with 0.1% TFA. The elute was diluted with EtOAc (10 mL) and then basified with saturated NaHCO₃. The organic layer was dried and concentrated to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-oxo-5-(piperazin-1-yl)pentyl 3-(3-fluorophenyl)isoxazol-5-ylcarbamate (0.2 g, 92%). LRMS (M+H⁺) m/z 605.1.

Example 53 Preparation of (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-oxo-5-(piperazin-1-yl)pentyl 5-(3-fluorophenyl)isoxazol-3-ylcarbamate

To a solution of (S)-tert-butyl 4-(4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-hydroxypentanoyl)piperazine-1-carboxylate (0.30 g, 0.6 mmol, 1.0 equiv.) in toluene (10 mL) at 100° C., was added 5-(3-fluorophenyl)isoxazole-3-carbonyl azide (0.13 g, 0.6 mmol, 1.0 equiv.). The mixture was stirred for 1 h. The solvent was removed and the residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (S)-tert-butyl 4-(4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(5-(3-fluorophenyl)isoxazol-3-ylcarbamoyloxy)pentanoyl)piperazine-1-carboxylate (0.3 g, 60%). LRMS (M+H⁺) m/z 705.1.

To a solution of (S)-tert-butyl 4-(4-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-(5-(3-fluorophenyl)isoxazol-3-ylcarbamoyloxy)pentanoyl)piperazine-1-carboxylate (0.3 g, 0.36 mmol, 1.0 equiv.) in MeOH (2 mL) at 0° C., was added HCl/dioxane (4 N, 0.9 mL, 3.6 mmol, 10 equiv.). The solution was stirred at RT for 1 h. The solvents were removed and the residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O with 0.1% TFA. The elute was diluted with EtOAc (10 mL) and then basified with saturated NaHCO₃. The organic layer was dried and concentrated to give (S)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-oxo-5-(piperazin-1-yl)pentyl 5-(3-fluorophenyl)isoxazol-3-ylcarbamate (0.18 g, 90%). LRMS (M+H⁺) m/z 605.1.

Example 54 Preparation of (S)-5-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,4-difluoropentyl 3-(3-fluorophenyl)isoxazol-5-ylcarbamate

To a solution of 4-nitrophenylchloroformate (1.62 g, 8 mmol) in THF (10 mL) was added a solution of 2-chloro-3-fluorobenzylamine (1.27 g, 8 mmol) and DIEA (2.78 mL, 16 mmol, 2.0 equiv.) in THF (10 mL). The resulting mixture was stirred at RT for 20 min and added into a mixture of (S)-5-azido-4,4-difluoro-2-(methylamino)pentan-1-ol (1.5 g, 8.0 mmol, 1.0 equiv.), DIEA (2.78 mL, 16 mmol) and THF (10 mL). The resulting mixture was stirred at RT for 1 h. The solvent was removed and purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (S)-1-(5-azido-4,4-difluoro-1-hydroxypentan-2-yl)-3-(2-chloro-3-fluorobenzyl)-1-methylurea (2.6 g, 86%) as a white solid. LRMS (M+H⁺) m/z 380.1.

To a solution of (S)-1-(5-azido-4,4-difluoro-1-hydroxypentan-2-yl)-3-(2-chloro-3-fluorobenzyl)-1-methylurea (0.30 g, 0.8 mmol, 1.0 equiv.) in toluene (20 mL) at 100° C., was added 3-(3-fluorophenyl)isoxazole-5-carbonyl azide (0.19 g, 0.8 mmol, 1.0 equiv.). The mixture was stirred at 100° C. for 1 h. The mixture was concentrated and purified on RP-HPLC using a mixture of acetonitrile and H₂O to give (S)-5-azido-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,4-difluoropentyl 3-(3-fluorophenyl)isoxazol-5-ylcarbamate (0.33 g, 71%) as a white solid. LRMS (M+H⁺) m/z 584.1.

To a mixture of (S)-5-azido-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,4-difluoropentyl 3-(3-fluorophenyl)isoxazol-5-ylcarbamate (0.35 g, 0.6 mmol) in MeOH (2 mL), was added 10% Pd/C (0.1 g). The mixture was transferred to an autoclave reactor, charged with 10 psi of hydrogen, and stirred for 10 mM. The catalyst was filtered off and the filtrate was concentrated. The residue was purified on RP-HPLC using a mixture of acetonitrile and H₂O with 0.1% TFA. The elute was washed with saturated NaHCO₃. The organic layer was concentrated to give (S)-5-amino-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-4,4-difluoropentyl 3-(3-fluorophenyl)isoxazol-5-ylcarbamate (0.18 g, 54%) as a white solid. LRMS (M+H⁺) m/z 558.1.

Example 55

Screening assays were performed using a pyruvate kinase and lactate dehydrogenase-coupled ATPase assay containing the following reagents: Potassium PIPES (50 mM), MgCl₂ (3 mM), KCl (100 mM), ATP (0.15 mM), DTT (1 mM), BSA (0.1 mg/ml), NADH (0.5 mM), PEP (1.5 mM), pyruvate kinase (4 U/ml), lactate dehydrogenase (8 U/ml), and antifoam (50 ppm) (concentrations expressed are final assay concentrations). The pH was adjusted to 6.80 at 22° C. by addition of potassium hydroxide. Lead optimization assays were performed with a more sensitive pyruvate kinase/horseradish peroxidase/pyruvate oxidase-coupled ATPase assay containing the following reagents: Potassium PIPES (12 mM), MgCl₂ (2 mM), KCl (100 mM), ATP (0.15 mM), BSA (0.05 mg/ml), potassium phosphate (2 mM), amplex red (0.1 mM), PEP (0.1 mM), pyruvate kinase (4 U/ml), horseradish peroxidase (0.5 U/ml), pyruvate oxidase (0.5 U/ml), and antifoam (50 ppm) (concentrations expressed are final assay concentrations). The pH was adjusted to 7.00 at 22° C. by addition of potassium hydroxide.

The protein components specific to this assay are chicken gizzard smooth muscle myosin subfragment-1 that has been chemically crosslinked to either cardiac or skeletal actin using an excess of 1-Ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride and N-hydroxysuccinimide. The exact concentration of the crosslinked smooth muscle myosin in the assay is determined empirically, by titration to achieve a desired rate of ATP hydrolysis. The concentration varies between protein preparations due to variations in the fraction of active molecules in each preparation.

Compound dose response assays are performed by first preparing a dilution series of test compound, each with an assay mixture containing potassium PIPES, MgCl₂, KCl, ATP, BSA, potassium phosphate, amplex red, PEP, crosslinked smooth muscle actomyosin (subfragment-1), antifoam, and water. The assay is started by adding an equal volume of solution containing potassium Pipes, MgCl₂, KCl, BSA, potassium phosphate, pyruvate kinase, horseradish peroxidase, pyruvate oxidase, antifoam, and water. ATP hydrolysis is monitored by measuring the fluorescence of amplex red (excitation at 480 nm, emission at 615 nm). The resulting dose response curve is fit by the 4 parameter equation y=Bottom+((Top-Bottom)/(1+((IC₅₀/X)^Hill))). The IC₅₀ is defined as the concentration at which ATPase activity is midway between the top and bottom of the dose response curve.

Certain chemical entities described herein have an IC₅₀ less than 10 μM; for example, less than 1 μM.

Example 56

Using procedures similar to those described herein, the compounds in the following table were synthesized and tested.

m/z M + H ChemicalName 438.1 N-[(2-chlorophenyl)methyl](4-{[N-(1-ethyl(4- piperidyl))carbamoyloxy]methyl}(2H-3,4,5,6-tetrahydropyran-4- yl))carboxamide 500.1 N-[(2-chlorophenyl)methyl](4-{[N-(4-methyl-2-phenyl(1,3-thiazol-5- yl))carbamoyloxy]methyl}(2H-3,4,5,6-tetrahydropyran-4- yl))carboxamide 465.1 {1-(2-aminoacetyl)-4-[(N-(2-thienyl)carbamoyloxy)methyl](4- piperidyl)}-N-[(2-chlorophenyl)methyl]carboxamide 479.0 (tert-butoxy)-N-[2-(4-{N-[(2-chlorophenyl)methyl]carbamoyl}-4-{[N-(4- M + H⁺ − Boc methyl(2-thienyl))carbamoyloxy]methyl}piperidyl)-2- oxoethyl]carboxamide 377.0 {[(2-chlorophenyl)methyl]amino}-N-methyl-N-{2-[N-(6-methyl(3- pyridyl))carbamoyloxy]ethyl}carboxamide 397.0 N-(4,5-dimethyl(1,3-thiazol-2-yl))[2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)ethoxy]carboxamide 383.0 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(5-methyl(1,3-thiazol-2-yl))carboxamide 376.9 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(5-methyl(2-pyridyl))carboxamide 431.1 {[(2-chlorophenyl)methyl]amino}-N-methyl-N-(2-{N-[6- (trifluoromethyl)(3-pyridyl)]carbamoyloxy}ethyl)carboxamide 378.0 {[(2-chlorophenyl)methyl]amino}-N-methyl-N-{2-[N-(5-methylpyrazin- 2-yl)carbamoyloxy]ethyl}carboxamide 433.0 {[(2-chlorophenyl)methyl]amino}-N-methyl-N-{2-[N-(4- methylbenzothiazol-2-yl)carbamoyloxy]ethyl}carboxamide 384.1 {[(2-chlorophenyl)methyl]amino}-N-methyl-N-{2-[N-(5-methyl(1,3,4- thiadiazol-2-yl))carbamoyloxy]ethyl}carboxamide 446.1 {[(2-chlorophenyl)methyl]amino}-N-methyl-N-{2-[N-(5-phenyl(1,3,4- thiadiazol-2-yl))carbamoyloxy]ethyl}carboxamide 398.1 {[(2-chlorophenyl)methyl]amino}-N-{2-[N-(5-ethyl(1,3,4-thiadiazol-2- yl))carbamoyloxy]ethyl}-N-methylcarboxamide 437.9 {[(2-chlorophenyl)methyl]amino}-N-methyl-N-(2-{N-[5- (trifluoromethyl)(1,3,4-thiadiazol-2-yl)]carbamoyloxy}ethyl)carboxamide 366.9 {[(2-chlorophenyl)methyl]amino}-N-methyl-N-{2-[N-(5-methylisoxazol- 3-yl)carbamoyloxy]ethyl}carboxamide 367.2 {[(2-chlorophenyl)methyl]amino}-N-methyl-N-{2-[N-(3-methylisoxazol- 5-yl)carbamoyloxy]ethyl}carboxamide 444.1 N-{2-[N-(5-bromopyrimidin-2-yl)carbamoyloxy]ethyl}{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 443.9 N-{2-[N-(5-bromopyrazin-2-yl)carbamoyloxy]ethyl}{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 388.2 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(5-cyano(2-pyridyl))carboxamide 431.2 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-[5-(trifluoromethyl)(2-pyridyl)]carboxamide 381.0 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(5-fluoro(2-pyridyl))carboxamide 442.9 N-(5-bromo(2-pyridyl))[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carboxamide 377.1 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(4-methyl(2-pyridyl))carboxamide 363.1 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(2-pyridyl)carboxamide 439.0 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(5-phenyl(2-pyridyl))carboxamide 389.1 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(5-vinyl(2-pyridyl))carboxamide 391.0 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(5-ethyl(2-pyridyl))carboxamide 357.1 N-(5-ethyl(2-pyridyl))(2-{N- methyl[benzylamino]carbonylamino}ethoxy)carboxamide 419.1 N-[2-(N-benzothiazol-2-ylcarbamoyloxy)ethyl]{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 433.1 {[(2-chlorophenyl)methyl]amino}-N-methyl-N-{2-[N-(6- methylbenzothiazol-2-yl)carbamoyloxy]ethyl}carboxamide 421.0 methyl 6-{[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carbonylamino}pyridine-3-carboxylate 428.2 {[(2-chlorophenyl)methyl]amino}-N-methyl-N-{2-[N-(1-phenylpyrazol- 3-yl)carbamoyloxy]ethyl}carboxamide 430.1 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(5-phenyl(1,3,4-oxadiazol-2-yl))carboxamide 409.1 N-[5-(tert-butyl)isoxazol-3-yl][2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carboxamide 403.1 N-benzo[d]isoxazol-3-yl[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carboxamide 402.1 N-benzimidazol-2-yl[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carboxamide 406.1 6-{[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carbonylamino}pyridine-3-carboxamide 393.0 {[(2-chlorophenyl)methyl]amino}-N-(2-{N-[5-(hydroxymethyl)(2- pyridyl)]carbamoyloxy}ethyl)-N-methylcarboxamide 405.1 N-{2-[N-(5-acetyl(2-pyridyl))carbamoyloxy]ethyl}{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 407.1 {[(2-chlorophenyl)methyl]amino}-N-(2-{N-[5-(hydroxyethyl)(2- pyridyl)]carbamoyloxy}ethyl)-N-methylcarboxamide 421.1 {[(2-chlorophenyl)methyl]amino}-N-(2-{N-[5-(1-hydroxy-isopropyl)(2- pyridyl)]carbamoyloxy}ethyl)-N-methylcarboxamide 413.0 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(3-isoquinolyl)carboxamide 413.2 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(2-quinolyl)carboxamide 575.0 (1-(2-aminoacetyl)-4-{[N-(5-bromo(2-pyridyl))carbamoyloxy]methyl}(4- piperidyl))-N-[(2,3-dichlorophenyl)methyl]carboxamide 413.1 {[(2-chlorophenyl)methyl]amino}-N-methyl-N-[2-(N-(6- quinolyl)carbamoyloxy)ethyl]carboxamide 419.2 N-[2-(N-benzothiazol-6-ylcarbamoyloxy)ethyl]{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 510.2 {1-(2-aminoacetyl)-4-[(N-(2-quinolyl)carbamoyloxy)methyl](4- piperidyl)}-N-[(2-chlorophenyl)methyl]carboxamide 530.1 (1-(2-aminoacetyl)-4-{[N-(4-methylbenzothiazol-2- yl)carbamoyloxy]methyl}(4-piperidyl))-N-[(2- chlorophenyl)methyl]carboxamide 536.2 (1-(2-aminoacetyl)-4-{[N-(5-phenyl(2-pyridyl))carbamoyloxy]methyl}(4- piperidyl))-N-[(2-chlorophenyl)methyl]carboxamide 474.1 (1-(2-aminoacetyl)-4-{[N-(5-methyl(2-pyridyl))carbamoyloxy]methyl}(4- piperidyl))-N-[(2-chlorophenyl)methyl]carboxamide 543.1 (1-(2-aminoacetyl)-4-{[N-(5-phenyl(1,3,4-thiadiazol-2- yl))carbamoyloxy]methyl}(4-piperidyl))-N-[(2- chlorophenyl)methyl]carboxamide 510.1 {1-(2-aminoacetyl)-4-[(N-(3-isoquinolyl)carbamoyloxy)methyl](4- piperidyl)}-N-[(2-chlorophenyl)methyl]carboxamide 530.1 (1-(2-aminoacetyl)-4-{[N-(6-methylbenzothiazol-2- yl)carbamoyloxy]methyl}(4-piperidyl))-N-[(2- chlorophenyl)methyl]carboxamide 584.1 [1-(2-aminoacetyl)-4-({N-[6-(trifluoromethyl)benzothiazol-2- yl]carbamoyloxy}methyl)(4-piperidyl)]-N-[(2- chlorophenyl)methyl]carboxamide 449.0 N-[2-(N-benzothiazol-2-ylcarbamoyloxy)ethyl]{[(2- chlorophenyl)methyl]amino}-N-(2-hydroxyethyl)carboxamide 441.1 [(2S)-2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)butoxy]-N-(3-isoquinolyl)carboxamide 461.1 [(2S)-2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)butoxy]-N-(6-methylbenzothiazol-2- yl)carboxamide 414.1 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-quinoxalin-2-ylcarboxamide 447.0 N-(5,6-dimethylbenzothiazol-2-yl)[2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)ethoxy]carboxamide 497.0 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-[6-(methylsulfonyl)benzothiazol-2-yl]carboxamide 503.0 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-[6-(trifluoromethoxy)benzothiazol-2-yl]carboxamide 486.9 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-[6-(trifluoromethyl)benzothiazol-2-yl]carboxamide 491.0 ethyl 2-{[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carbonylamino}benzothiazole-6- carboxylate 449.0 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(6-methoxybenzothiazol-2-yl)carboxamide 449.0 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(4-methoxybenzothiazol-2-yl)carboxamide 487.9 N-(5,6-dichlorobenzothiazol-2-yl)[2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)ethoxy]carboxamide 420.1 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(1,3-thiazolo[5,4-b]pyridin-2-yl)carboxamide 462.1 2-{[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carbonylamino}benzothiazole-6- carboxamide 447.1 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(5-(3-pyridyl)(1,3,4-thiadiazol-2-yl))carboxamide 447.1 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(5-(4-pyridyl)(1,3,4-thiadiazol-2-yl))carboxamide 455.1 [(2S)-2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-3- methylbutoxy]-N-(3-isoquinolyl)carboxamide 475.1 [(2S)-2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-3- methylbutoxy]-N-(6-methylbenzothiazol-2-yl)carboxamide 469.1 [(2S)-2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-4- methylpentyloxy]-N-(3-isoquinolyl)carboxamide 489 [(2S)-2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-4- methylpentyloxy]-N-(6-methylbenzothiazol-2-yl)carboxamide 512.1 {[(2-chlorophenyl)methyl]amino}-N-[2-(3-diazo-3-azaprop-3- enyloxy)ethyl]-N-[2-(N-(3-isoquinolyl)carbamoyloxy)ethyl]carboxamide 486.2 N-[2-(2-aminoethoxy)ethyl]{[(2-chlorophenyl)methyl]amino}-N-[2-(N- (3-isoquinolyl)carbamoyloxy)ethyl]carboxamide 528.2 {[(2-chlorophenyl)methyl]amino}-N-[2-(N-(3- isoquinolyl)carbamoyloxy)ethyl]-N-{2-[2- (trimethylamino)ethoxy]ethyl}carboxamide 423.1 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(4,5,6,7-tetrahydrobenzothiazol-2-yl)carboxamide 429.1 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(4-hydroxy(2-quinolyl))carboxamide 413.1 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(3-quinolyl)carboxamide 444.1 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(6-methyl-4-oxo(3-hydroquinazolin-2-yl))carboxamide 561.2 phenylmethyl (3S)-3-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)-4-(N-(3-isoquinolyl)carbamoyloxy)butanoate 581.1 phenylmethyl (3S)-3-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-methylbenzothiazol-2- yl)carbamoyloxy]butanoate 457.1 [(2S)-2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-4- hydroxybutoxy]-N-(3-isoquinolyl)carboxamide 485.1 methyl (3S)-3-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)-4-(N-(3-isoquinolyl)carbamoyloxy)butanoate 488.2 {[(2-chlorophenyl)methyl]amino}-N-[2-(2-hydroxyethoxy)ethyl]-N-[2- (N-(3-isoquinolyl)carbamoyloxy)ethyl]carboxamide 514.2 N-{2-[2-(dimethylamino)ethoxy]ethyl}{[(2-chlorophenyl)methyl]amino}- N-[2-(N-(3-isoquinolyl)carbamoyloxy)ethyl]carboxamide 500.2 {[(2-chlorophenyl)methyl]amino}-N-[2-(N-(3- isoquinolyl)carbamoyloxy)ethyl]-N-{2-[2- (methylamino)ethoxy]ethyl}carboxamide 411.2 4-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-N-(3- isoquinolyl)butanamide 397.1 3-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-N-(3- isoquinolyl)propanamide 575.2 phenylmethyl (4S)-4-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)pentanoate 499.1 methyl (4S)-4-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)pentanoate 427.1 [(2R)-2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-(3-isoquinolyl)carboxamide 427.1 {[(2-chlorophenyl)methyl]methylamino}-N-[2-(N-(3- isoquinolyl)carbamoyloxy)ethyl]-N-methylcarboxamide 472.2 [2-(N-((2R)-2-amino-3-hydroxypropyl){[(2- chlorophenyl)methyl]amino}carbonylamino)ethoxy]-N-(3- isoquinolyl)carboxamide 427.1 [(2S)-2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-(3-isoquinolyl)carboxamide 471.0 [(2S)-2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-5- hydroxypentyloxy]-N-(3-isoquinolyl)carboxamide 433.1 N-{(1S)-2-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]ethyl}{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 421.0 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]propyl}-N- methyl{[(2-methylphenyl)methyl]amino}carboxamide 403.0 N-benzoxazol-2-yl[2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carboxamide 455.0 N-(5,6-difluorobenzothiazol-2-yl)[2-({[(2-chlorophenyl)methyl]amino}- N-methylcarbonylamino)ethoxy]carboxamide 513.1 methyl (5S)-5-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3-isoquinolyl)carbamoyloxy)hexanoate 499.1 (5S)-5-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-6- (N-(3-isoquinolyl)carbamoyloxy)hexanoic acid 485.2 N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]pentyl}{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 510.2 N-{(1S)-6-diazo-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-6-azahex-6- enyl}{[(2-chlorophenyl)methyl]amino}-N-methylcarboxamide 484.2 N-{(1S)-5-amino-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]pentyl}{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 533.2 N-{(1S)-2-(N-(3-isoquinolyl)carbamoyloxy)-1- [(phenylmethoxy)methyl]ethyl}{[(2-chlorophenyl)methyl]amino}-N- methylcarboxamide 499.2 N-{(1S)-2-(N-(3-isoquinolyl)carbamoyloxy)-1- [(phenylmethoxy)methyl]ethyl}-N-methyl[benzylamino]carboxamide 471.2 (3S)-3-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-4- (N-(3-isoquinolyl)carbamoyloxy)butanoic acid 485.2 [(2R)-2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-6- hydroxyhexyloxy]-N-(3-isoquinolyl)carboxamide 485.2 N-{(1S)-3-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-3- methylbutyl}{[(2-chlorophenyl)methyl]amino}-N-methylcarboxamide 514.1 (3S)-3-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-4- (N-(3-isoquinolyl)carbamoyloxy)-N-methoxy-N-methylbutanamide 526.2 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-3-morpholin-4- ylpropyl}{[(2-chlorophenyl)methyl]amino}-N-methylcarboxamide 513.2 N-{(1S)-5-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2-chlorophenyl)methyl]amino}-N-methylcarboxamide 497.2 N-{(1S)-5-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2-fluorophenyl)methyl]amino}-N-methylcarboxamide 539.2 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-3-(4- methylpiperazinyl)propyl}{[(2-chlorophenyl)methyl]amino}-N- methylcarboxamide 567.3 N-{(1S)-3-(4-acetylpiperazinyl)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]propyl}{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 597.3 ethyl 4-[(3S)-3-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)-4-(N-(3- isoquinolyl)carbamoyloxy)butyl]piperazinecarboxylate 603.3 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-3-[4- (methylsulfonyl)piperazinyl]propyl}{[(2-chlorophenyl)methyl]amino}-N- methylcarboxamide 531.2 methyl (5S)-5-({[(2-chloro-4-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3-isoquinolyl)carbamoyloxy)hexanoate 531.2 methyl (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3-isoquinolyl)carbamoyloxy)hexanoate 471.2 N-{(1S,3S)-3-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 471.2 N-{(1S,3R)-3-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 499.3 N-{(1S)-4-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4- methylpentyl}{[(2-chlorophenyl)methyl]amino}-N-methylcarboxamide 503.5 N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]pentyl}{[(2-chloro-4- fluorophenyl)methyl]amino}-N-methylcarboxamide 531.3 N-{(1S)-5-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2-chloro-4-fluorophenyl)methyl]amino}-N- methylcarboxamide 503.2 N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]pentyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 470.2 [(2S)-5-amino-2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)pentyloxy]-N-(3-isoquinolyl)carboxamide 515.2 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3-isoquinolyl)carbamoyloxy)hexanoate 547.2 methyl (5S)-5-({[(2,3-dichlorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3-isoquinolyl)carbamoyloxy)hexanoate 531.2 methyl (5S)-5-({[(3-chloro-2-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3-isoquinolyl)carbamoyloxy)hexanoate 487.2 N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]pentyl}{[(2,3- difluorophenyl)methyl]amino}-N-methylcarboxamide 485.2 N-{(1S)-4-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]pentyl}{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 542.3 (5S)-5-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-6- (N-(3-isoquinolyl)carbamoyloxy)-N-methoxy-N-methylhexanamide 497.2 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-5-oxohexyl}{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 499.2 N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]hexyl}{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 519.2 N-{(1S)-5-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]pentyl}{[(2,3- dichlorophenyl)methyl]amino}-N-methylcarboxamide 531.2 N-{(1S)-5-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 547.2 N-{(1S)-5-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2,3-dichlorophenyl)methyl]amino}-N- methylcarboxamide 515.2 N-{(1S)-5-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 531.2 N-{(1S)-5-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(3-chloro-2-fluorophenyl)methyl]amino}-N- methylcarboxamide 515.2 N-{(1S)-5-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2,4-difluorophenyl)methyl]amino}-N- methylcarboxamide 547.2 N-{(1S)-5-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-5- methylhexyl}{[(2,4-dichlorophenyl)methyl]amino}-N- methylcarboxamide 527.2 [(2S)-2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-4- hydroxy-4-methylpentyloxy]-N-(5,6-difluorobenzothiazol-2- yl)carboxamide 503.2 N-{(1S)-3-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-3- methylbutyl}{[(2-chloro-4-fluorophenyl)methyl]amino}-N- methylcarboxamide 513.1 (3S)-4-[N-(5,6-difluorobenzothiazol-2-yl)carbamoyloxy]-3-({[(2- chlorophenyl)methyl]amino}-N-methylcarbonylamino)butanoic acid 527.2 methyl (3S)-4-[N-(5,6-difluorobenzothiazol-2-yl)carbamoyloxy]-3-({[(2- chlorophenyl)methyl]amino}-N-methylcarbonylamino)butanoate 526.2 N-[(5S)-5-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)- 6-(N-(3-isoquinolyl)carbamoyloxy)hexyl]acetamide 402.0 {[(2-chlorophenyl)methyl]amino}-N-[2-(N-(4-hydroimidazo[1,2- a]pyridin-2-yl)carbamoyloxy)ethyl]-N-methylcarboxamide 545.2 N-((1S)-1-{[N-(5,6-difluorobenzothiazol-2-yl)carbamoyloxy]methyl}-3- hydroxy-3-methylbutyl){[(2-chloro-4-fluorophenyl)methyl]amino}-N- methylcarboxamide 402.0 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(8-hydropyrazolo[1,5-a]pyridin-2-yl)carboxamide 620.2 N-[(5S)-5-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)- 6-(N-(3-isoquinolyl)carbamoyloxy)hexyl]-2-diazo-3,3,3- trifluoropropanamide 545.2 N-((1S)-1-{[N-(5,6-difluorobenzothiazol-2-yl)carbamoyloxy]methyl}-3- hydroxy-3-methylbutyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 545.2 N-((1S)-1-{[N-(5,6-difluorobenzothiazol-2-yl)carbamoyloxy]methyl}-3- hydroxy-3-methylbutyl){[(3-chloro-2-fluorophenyl)methyl]amino}-N- methylcarboxamide 471.2 N-{(1R)-2-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-2- methylpropyl}{[(2-chlorophenyl)methyl]amino}-N-methylcarboxamide 471.2 methyl (2R)-2-({[(2-chlorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3-isoquinolyl)carbamoyloxy)propanoate 522.1 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-3- hydroxy-3-methylbutyl){[(2-chloro-4-fluorophenyl)methyl]amino}-N- methylcarboxamide 522.1 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-3- hydroxy-3-methylbutyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 503.2 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-3- hydroxy-3-methylbutyl){[(2-chlorophenyl)methyl]amino}-N- methylcarboxamide 503.1 N-{(1S)-3-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-3- methylbutyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 402.1 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-(8-hydropyrrolo[1,2-e]pyrimidin-3-yl)carboxamide 543.1 N-{(1S)-2-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-1-[(3- oxopiperazinyl)methyl]ethyl}{[(2-chlorophenyl)methyl]amino}-N- methylcarboxamide 543.2 N-{(1S)-2-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-1-[(4- methylpiperazinyl)methyl]ethyl}{[(2-chlorophenyl)methyl]amino}-N- methylcarboxamide 512.2 N-[(1S)-2-(N-(3-isoquinolyl)carbamoyloxy)-1-(morpholin-4- ylmethyl)ethyl]{[(2-chlorophenyl)methyl]amino}-N-methylcarboxamide 557.2 [(2S)-2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-3- (4-methyl-3-oxopiperazinyl)propoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 517.2 [(2S)-2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-4- hydroxy-3,4-dimethylpentyloxy]-N-(6-fluoro(3-isoquinolyl))carboxamide 517.2 [(2S)-2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-4- hydroxy-3,4-dimethylpentyloxy]-N-(6-fluoro(3-isoquinolyl))carboxamide 506.2 N-{(1S)-1-[(dimethylamino)methyl]-2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 475.0 [((2S)-1-{N-[(2-chloro-4-fluorophenyl)methyl]carbamoyl}pyrrolidin-2- yl)methoxy]-N-(6-fluoro(3-isoquinolyl))carboxamide 521.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-hydroxy-4-methylpentyloxy]-N-(5-fluoro(3- isoquinolyl))carboxamide 521.2 [(2S)-2-({[(2-chloro-4-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-hydroxy-4-methylpentyloxy]-N-(5-fluoro(3- isoquinolyl))carboxamide 503.2 [(2S)-2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-4- hydroxy-4-methylpentyloxy]-N-(5-fluoro(3-isoquinolyl))carboxamide 553.2 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-3-(4-methyl-3- oxopiperazinyl)propyl}{[(2-chlorophenyl)methyl]amino}-N- methylcarboxamide 539.2 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-3-(3- oxopiperazinyl)propyl}{[(2-chlorophenyl)methyl]amino}-N- methylcarboxamide 521.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-hydroxy-4-methylpentyloxy]-N-(7-fluoro(3- isoquinolyl))carboxamide 521.2 [(2S)-2-({[(2-chloro-4-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-hydroxy-4-methylpentyloxy]-N-(7-fluoro(3- isoquinolyl))carboxamide 503.2 [(2S)-2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-4- hydroxy-4-methylpentyloxy]-N-(7-fluoro(3-isoquinolyl))carboxamide 463.2 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-ethyl-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}carboxamide 477.0 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-N-(methylethyl)carboxamide 463.2 {[(2-chloro-4-fluorophenyl)methyl]amino}-N-ethyl-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}carboxamide 477.0 {[(2-chloro-4-fluorophenyl)methyl]amino}-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-N-(methylethyl)carboxamide 549.2 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-3- hydroxy-3-methylbutyl){[(2-chloro-4-fluorophenyl)methyl]amino}-N- (methylethyl)carboxamide 531.2 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-3- hydroxy-3-methylbutyl){[(2-chlorophenyl)methyl]amino}-N- (methylethyl)carboxamide 475.0 [((2S)-1-{N-[(2-chloro-4-fluorophenyl)methyl]carbamoyl}pyrrolidin-2- yl)methoxy]-N-(8-hydropyrrolo[1,2-e]pyrimidin-3-yl)carboxamide 416.0 [2-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)ethoxy]- N-pyridino[4,3-d]pyridin-3-ylcarboxamide 475.0 [((2S)-1-{N-[(2-chloro-3-fluorophenyl)methyl]carbamoyl}pyrrolidin-2- yl)methoxy]-N-(6-fluoro(3-isoquinolyl))carboxamide 507.1 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-N-(2-hydroxy-2- methylpropyl)carboxamide 517.1 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-N-(2,2,2-trifluoroethyl)carboxamide 461.0 {[(2-chloro-3-methoxyphenyl)methyl]amino}-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-N-methylcarboxamide 517.1 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-3- hydroxy-3-methylbutyl){[(2-chlorophenyl)methyl]amino}-N- ethylcarboxamide 535.2 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-3- hydroxy-3-methylbutyl){[(2-chloro-4-fluorophenyl)methyl]amino}-N- ethylcarboxamide 596.2 N-((1S)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-4- fluorophenyl)methyl]amino}-N-methylcarboxamide 533.2 N-((1S)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2- bromophenyl)methyl]amino}-N-methylcarboxamide 557.2 N-(2-aminoethyl)(4-{N-[(2-chlorophenyl)methyl]carbamoyl}-4-{[N-(6- fluoro(3-isoquinolyl))carbamoyloxy]methyl}piperidyl)carboxamide 645.3 (tert-butoxy)-N-[2-(4-{N-[(2-bromophenyl)methyl]carbamoyl}-4-{[N-(4- ethylphenyl)carbamoyloxy]methyl}piperidyl)-2-oxoethyl]-N- methylcarboxamide 545.2 [(4-{N-[(2-bromophenyl)methyl]carbamoyl}-1-[2- (methylamino)acetyl](4-piperidyl))methoxy]-N-(4- ethylphenyl)carboxamide 499.0 N-(2,2-difluoroethyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N-{2- [N-(6-fluoro(3-isoquinolyl))carbamoyloxy]ethyl}carboxamide 531.0 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-N-(3,3,3-trifluoropropyl)carboxamide MS: [((2S,4R)-1-{N-[(2-chloro-3-fluorophenyl)methyl]carbamoyl}-4- 491.0 (M + 1) hydroxypyrrolidin-2-yl)methoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 458.0 [((2S)-1-{N-[(2-chloro-3-fluorophenyl)methyl]carbamoyl}pyrrolidin-2- yl)methoxy]-N-pyridino[4,3-d]pyridin-3-ylcarboxamide 447.1 {[(2-chloro-3-hydroxyphenyl)methyl]amino}-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-N-methylcarboxamide 474.0 (2-{1-[(2-chloro-4-fluorophenyl)methyl]-3-methyl-2-oxopyrrolidin-3- yl}ethoxy)-N-(6-fluoro(3-isoquinolyl))carboxamide 506.1 N-((1S)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 491.1 ((5S,3R)-1-{N-[(2-chloro-3-fluorophenyl)methyl]carbamoyl}-5- (hydroxymethyl)pyrrolidin-3-yloxy)-N-(6-fluoro(3- isoquinolyl))carboxamide 474.1 {[((2S)-1-{N-[(2-chloro-3-fluorophenyl)methyl]carbamoyl}pyrrolidin-2- yl)methyl]amino}-N-(6-fluoro(3-isoquinolyl))carboxamide 489.0 methyl 2-chloro-3-{[(N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-N- methylcarbamoyl)amino]methyl}benzoate 491.2 4-amino-N-[(2-chloro-4-fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-2-methylbutanamide 488.2 N-((1S)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 552.2 N-((1S)-4-[(2,2-difluoroethyl)amino]-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 490.0 [((2S,4R)-4-amino-1-{N-[(2-chloro-3- fluorophenyl)methyl]carbamoyl}pyrrolidin-2-yl)methoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 647.1 N-((5S,3R)-1-{N-[(2-chloro-3-fluorophenyl)methyl]carbamoyl}-5-{[N- (6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}pyrrolidin-3-yl)-2-[(tert- butoxy)carbonylamino]acetamide 547.0 N-((5S,3R)-1-{N-[(2-chloro-3-fluorophenyl)methyl]carbamoyl}-5-{[N- (6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}pyrrolidin-3-yl)-2- aminoacetamide 461.0 [((2S)-1-{N-[(2-chloro-3-fluorophenyl)methyl]carbamoyl}azetidin-2- yl)methoxy]-N-(6-fluoro(3-isoquinolyl))carboxamide 489.2 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}but-3- enyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide 523.2 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-3,4- dihydroxybutyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 606.2 N-((1S)-4-[(tert-butoxy)carbonylamino]-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 488.1 N-{(1S)-4-amino-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]butyl}{[(2- chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide 488.2 N-{(1S)-4-amino-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]butyl}{[(2- chloro-4-fluorophenyl)methyl]amino}-N-methylcarboxamide 504.2 N-{(1S)-4-amino-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2,3- dichlorophenyl)methyl]amino}-N-methylcarboxamide 461.2 ({[2-chloro-3-(hydroxymethyl)phenyl]methyl}amino)-N-{2-[N-(6- fluoro(3-isoquinolyl))carbamoyloxy]ethyl}-N-methylcarboxamide 462.2 N-[(2-chloro-3-fluorophenyl)methyl]-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-2,2-dimethylbutanamide 488.2 N-[(2-chloro-3-fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-2-methylpent-4-enamide 522.2 N-[(2-chloro-3-fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-4,5-dihydroxy-2-methylpentanamide 506.2 N-[(2-chloro-3-fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-5-hydroxy-2-methylpentanamide 465.1 {[(2,5-dichlorophenyl)methyl]amino}-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-N-methylcarboxamide 449.2 {[(5-chloro-2-fluorophenyl)methyl]amino}-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-N-methylcarboxamide 535.2 methyl (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanoate 549.2 ethyl (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanoate 564.2 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-N- methoxy-N-methylpentanamide 552.2 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-4-[(2- fluoroethyl)amino]butyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 570.2 N-((1S)-4-[(2,2-difluoroethyl)amino]-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 588.2 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-4-[(2,2,2- trifluoroethyl)amino]butyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 582.2 N-((1S)-4-(3,3-difluoroazetidinyl)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 596.2 N-((1S)-4-(3,3-difluoropyrrolidinyl)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 507.2 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-4- hydroxybutyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 448.2 N-[(2-chloro-3-fluorophenyl)methyl]-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]-2-methylbutanamide 503.2 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-5- hydroxypentyl){[(2-chlorophenyl)methyl]amino}-N-methylcarboxamide 521.2 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-5- hydroxypentyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 523.2 N-((1S,3S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-3,4- dihydroxybutyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 523.2 N-((1S,3R)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-3,4- dihydroxybutyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 648.1 4-{2-[(tert-butoxy)carbonylamino]acetylamino}-N-[(2-chloro-3- fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-2-methylbutanamide 548.1 4-(2-aminoacetylamino)-N-[(2-chloro-3-fluorophenyl)methyl]-2-{2-[N- (6-fluoro(3-isoquinolyl))carbamoyloxy]ethyl}-2-methylbutanamide 505.2 5-amino-N-[(2-chloro-3-fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-2-methylpentanamide 520.2 N-[(2-chloro-3-fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-6-hydroxy-2-methylhexanamide 562.2 5-(2-aminoacetylamino)-N-[(2-chloro-3-fluorophenyl)methyl]-2-{2-[N- (6-fluoro(3-isoquinolyl))carbamoyloxy]ethyl}-2-methylpentanamide 522.2 N-((1S)-4-amino-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}- 3-hydroxybutyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 474.2 N-{2-[N-(5-bromo-4-methyl(2-pyridyl))carbamoyloxy]ethyl}{[(2-chloro- 3-fluorophenyl)methyl]amino}-N-methylcarboxamide 413.2 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-{2-[N-(5-fluoro-4- methyl(2-pyridyl))carbamoyloxy]ethyl}-N-methylcarboxamide 395.2 {[(2-chlorophenyl)methyl]amino}-N-{2-[N-(5-fluoro-4-methyl(2- pyridyl))carbamoyloxy]ethyl}-N-methylcarboxamide 520.2 N-((1S)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}pentyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 490.2 N-[(2-chloro-3-fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-2-methylpentanamide 593.2 (2S)-N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]-2-amino-3-hydroxypropanamide 593.2 (2R)-N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]-2-amino-3-hydroxypropanamide 563.2 N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]-2-aminoacetamide 538.2 N-((1S)-4-amino-5,5-difluoro-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}pentyl){[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 492.2 N-[(2-chloro-3-fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-4-hydroxy-2-methylbutanamide 634.3 2-({2-[(tert-butoxy)carbonylamino]acetylamino}methyl)-N-[(2-chloro-3- fluorophenyl)methyl]-4-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- methylbutanamide 534.2 2-[(2-aminoacetylamino)methyl]-N-[(2-chloro-3-fluorophenyl)methyl]-4- [N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2-methylbutanamide 449.2 {[(2-chloro-5-fluorophenyl)methyl]amino}-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-N-methylcarboxamide 591.1 2-{2-[(tert-butoxy)carbonylamino]ethyl}-N-[(2-chloro-3- fluorophenyl)methyl]-4-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- methylbutanamide 491.1 4-amino-N-[(2-chloro-3-fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-2-methylbutanamide 549.0 N-[(2-chloro-3-fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-4-(2-hydroxyacetylamino)-2- methylbutanamide 678.1 4-{(2S)-2-[(tert-butoxy)carbonylamino]-3-hydroxypropanoylamino}-N- [(2-chloro-3-fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-2-methylbutanamide 578.1 4-((2S)-2-amino-3-hydroxypropanoylamino)-N-[(2-chloro-3- fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-2-methylbutanamide 579.1 4-(2,3-dihydroxypropanoylamino)-N-[(2-chloro-3-fluorophenyl)methyl]- 2-{2-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]ethyl}-2- methylbutanamide 519.2 6-amino-N-[(2-chloro-3-fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-2-methylhexanamide 491.2 [((2R,3R)-1-{N-[(2-chloro-3-fluorophenyl)methyl]carbamoyl}-3- hydroxypyrrolidin-2-yl)methoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 631.2 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl dimethyl phosphate 539.2 N-((1S,3S)-1-{[N-(6-fluoro-2-hydroxy(3- isoquinolyl))carbamoyloxy]methyl}-3,4-dihydroxybutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 539.2 N-((1S,3R)-1-{[N-(6-fluoro-2-hydroxy(3- isoquinolyl))carbamoyloxy]methyl}-3,4-dihydroxybutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 397.2 N-{2-[N-(5-chloro(2-pyridyl))carbamoyloxy]ethyl}{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 522.2 ({(4S)-6-(aminomethyl)-1-[(2-chloro-3-fluorophenyl)methyl]-6-fluoro-3- methyl-2-oxo(1,3-diazaperhydroin-4-yl)}methoxy)-N-(6-fluoro(3- isoquinolyl))carboxamide 556.2 N-((1S)-4-amino-5,5-difluoro-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}pentyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 690.2 N-((1S)-5,5-difluoro-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-4- [(phenylmethoxy)carbonylamino]pentyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 616.0 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl hydrogen methyl phosphate 521.2 N-((1S)-3,4-diamino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 576.1 6-(2-aminoacetylamino)-N-[(2-chloro-3-fluorophenyl)methyl]-2-{2-[N- (6-fluoro(3-isoquinolyl))carbamoyloxy]ethyl}-2-methylhexanamide 536.1 N-[(2-chloro-3-fluorophenyl)methyl]-2-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-5,6-dihydroxy-2-methylhexanamide 522.2 N-((1S,3R)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-3-hydroxybutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 522.2 N-((1S,3S)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-3-hydroxybutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 601.0 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl dihydrogen phosphate 555.2 2-{2-[(2,2-difluoroethyl)amino]ethyl}-N-[(2-chloro-3- fluorophenyl)methyl]-4-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- methylbutanamide 420.2 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-{2-[N-(5-cyano-4- methyl(2-pyridyl))carbamoyloxy]ethyl}-N-methylcarboxamide 409.2 N-{2-[N-(4,5-dimethyl(2-pyridyl))carbamoyloxy]ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 391.2 N-{2-[N-(4,5-dimethyl(2-pyridyl))carbamoyloxy]ethyl}{[(2- chlorophenyl)methyl]amino}-N-methylcarboxamide 608.3 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl 2-(dimethylamino)acetate 580.1 (3S)-N-(2,3-dihydroxypropyl)-3-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butanamide 649.2 (3S)-N-{2-[(tert-butoxy)carbonylamino]ethyl}-3-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butanamide 689.2 tert-butyl 4-[(3S)-3-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butanoylamino]piperidinecarboxylate 675.2 tert-butyl 4-[(3S)-3-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butanoyl]piperazinecarboxylate 549.1 (3S)-N-(2-aminoethyl)-3-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butanamide 589.2 (3S)-3-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-N- (4-piperidyl)butanamide 575.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-oxo-4-piperazinylbutoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 490.2 [((2S,3S)-3-amino-1-{N-[(2-chloro-3- fluorophenyl)methyl]carbamoyl}pyrrolidin-2-yl)methoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 516.0 [((2S,3S)-1-{N-[(2-chloro-3-fluorophenyl)methyl]carbamoyl}-3- (diazoazamvinyl)pyrrolidin-2-yl)methoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 509.1 N-{2-[N-(5-bromo(3-isoquinolyl))carbamoyloxy]ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 489.1 methyl 3-{[2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carbonylamino}isoquinoline-5-carboxylate 432.1 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-methyl-N-[2-(N- pyridino[3,4-d]pyridin-3-ylcarbamoyloxy)ethyl]carboxamide 507.1 (3S)-3-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butanoic acid 679.2 N-{(2R)-2-[(tert-butoxy)carbonylamino]-3-hydroxypropyl}(3S)-3-({[(2- chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-4-[N-(6- fluoro(3-isoquinolyl))carbamoyloxy]butanamide 579.1 N-((2R)-2-amino-3-hydroxypropyl)(3S)-3-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butanamide 576.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-morpholin-4-yl-4-oxobutoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 491.2 [((3S,2R)-1-{N-[(2-chloro-3-fluorophenyl)methyl]carbamoyl}-3- hydroxypyrrolidin-2-yl)methoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 535.2 N-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]propyl]-2-aminoacetamide 565.2 (2S)-N-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]propyl]-2-amino-3-hydroxypropanamide 565.2 (2R)-N-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]propyl]-2-amino-3-hydroxypropanamide 578.2 [(2S)-3-[(tert-butoxy)carbonylamino]-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)propoxy]-N-(6- fluoro(3-isoquinolyl))carboxamide 478.1 [(2S)-3-amino-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-(6-fluoro(3-isoquinolyl))carboxamide 606.2 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl 2-(dimethylamino)acetate 550.2 N-((1S)-5-diazo-3-fluoro-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-5-azapent-5-enyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 432.1 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-methyl-N-[2-(N- pyridino[2,3-d]pyridin-7-ylcarbamoyloxy)ethyl]carboxamide 461.2 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-(2-{N-[5- (hydroxymethyl)(3-isoquinolyl)]carbamoyloxy}ethyl)-N- methylcarboxamide 509.1 N-{2-[N-(8-bromo(3-isoquinolyl))carbamoyloxy]ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 473.2 N-{2-[N-(5-acetyl(3-isoquinolyl))carbamoyloxy]ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 474.2 3-{[2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carbonylamino}isoquinoline-5- carboxamide 524.2 N-((1S)-4-amino-3-fluoro-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 629.2 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl dimethyl phosphate 619.2 N-{(1S)-4-(1,3-dioxobenzo[c]azolin-2-yl)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 545.2 N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)pentyl]-2- aminoacetamide 575.2 (2S)-N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)pentyl]-2- amino-3-hydroxypropanamide 575.2 (2R)-N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)pentyl]-2- amino-3-hydroxypropanamide 592.2 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl 2-(dimethylamino)acetate 587.1 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl dihydrogen phosphate 492.1 [(2S)-4-amino-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)butoxy]-N-(6-fluoro(3-isoquinolyl))carboxamide 549.2 N-[(3S)-3-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butyl]-2-aminoacetamide 720.1 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl (2S)-2-[(tert-butoxy)carbonylamino]-3- methylbutanoate 720.1 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl (2R)-2-[(tert-butoxy)carbonylamino]-3- methylbutanoate 620.1 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl (2S)-2-amino-3-methylbutanoate 620.1 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl (2R)-2-amino-3-methylbutanoate 599.0 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl dihydrogen phosphate 548.1 N-((1S)-4-(amidinoamino)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 549.1 N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]aminoamide 587.2 N-(4-{[(1E)-2-cyano-1-(methylamino)-2-azavinyl]amino}(1S)-1-{[N-(6- fluoro(3-isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 594.2 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl (2S)-2-amino-3-hydroxypropanoate 594.1 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl (2R)-2-amino-3-hydroxypropanoate 606.2 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl (2S)-2-amino-3-methylbutanoate 606.2 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl (2R)-2-amino-3-methylbutanoate 432.2 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-methyl-N-[2-(N- pyridino[3,2-d]pyridin-6-ylcarbamoyloxy)ethyl]carboxamide 489.1 N-{(1S)-4-amino-1-[(N-pyridino[4,3-d]pyridin-3- ylcarbamoyloxy)methyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 489.1 N-{(1S)-4-amino-1-[(N-pyridino[3,2-d]pyridin-6- ylcarbamoyloxy)methyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 689.3 tert-butyl 4-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanoyl]piperazinecarboxylate 663.3 (4S)-N-{2-[(tert-butoxy)carbonylamino]ethyl}-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanamide 693.3 N-{(2R)-2-[(tert-butoxy)carbonylamino]-3-hydroxypropyl}(4S)-4-({[(2- chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-[N-(6- fluoro(3-isoquinolyl))carbamoyloxy]pentanamide 689.3 tert-butyl 3-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanoylamino]pyrrolidinecarboxylate 456.1 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-{2-[N-(8-cyano(3- isoquinolyl))carbamoyloxy]ethyl}-N-methylcarboxamide 563.2 (4S)-N-(2-aminoethyl)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanamide 589.2 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-4-oxo-4- piperazinylbutyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 593.2 N-((2R)-2-amino-3-hydroxypropyl)(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanamide 589.2 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-N- pyrrolidin-3-ylpentanamide 579.1 (2S)-N-[(3S)-3-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butyl]-2-amino-3-hydroxypropanamide 579.2 (2R)-N-[(3S)-3-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]butyl]-2-amino-3-hydroxypropanamide 573.2 N-(4-[((1E)-1-amino-2-cyano-2-azavinyl)amino](1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 591.2 N-(4-[((1E)-1-amino-2-carbamoyl-2-azavinyl)amino](1S)-1-{[N-(6- fluoro(3-isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 601.2 N-((1S)-4-{[(1Z)-1-(dimethylamino)-2-cyano-2-azavinyl]amino}-1-{[N- (6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 511.0 N-(6-bromo(3-isoquinolyl))[2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carboxamide 636.2 N-((1S)-4-(1,3-dioxobenzo[c]azolin-2-yl)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 676.2 (2S)-N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-pyridino[4,3-d]pyridin-3- ylcarbamoyloxy)pentyl]-2-[(tert-butoxy)carbonylamino]-3- hydroxypropanamide 576.2 (2S)-N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-pyridino[4,3-d]pyridin-3- ylcarbamoyloxy)pentyl]-2-amino-3-hydroxypropanamide 676.2 (2S)-N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-pyridino[3,2-d]pyridin-6- ylcarbamoyloxy)pentyl]-2-[(tert-butoxy)carbonylamino]-3- hydroxypropanamide 576.2 (2S)-N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-pyridino[3,2-d]pyridin-6- ylcarbamoyloxy)pentyl]-2-amino-3-hydroxypropanamide 739.2 (3S)-3-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-1- [(methoxyphosphinyl)methyl]butyl dimethyl phosphate 489.0 methyl 3-{[2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carbonylamino}isoquinoline-6-carboxylate 520.1 N-((1S)-3-carbamoyl-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}propyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 521.1 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanoic acid 517.2 methyl (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)pentanoate 506.1 N-[(1S)-4-amino-1-({N-[5-(trifluoromethyl)(2- pyridyl)]carbamoyloxy}methyl)butyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 519.1 N-((1S)-3-amidino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}propyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 547.1 N-((1S)-4-(ethylamino)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-4-iminobutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 503.2 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)pentanoic acid 509.0 N-(7-bromo(3-isoquinolyl))[2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carboxamide 572.3 (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 6-(N-(3-isoquinolyl)carbamoyloxy)hexyl 2-(dimethylamino)acetate 567.2 (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 6-(N-(3-isoquinolyl)carbamoyloxy)hexyl dihydrogen phosphate 586.3 (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 6-(N-(3-isoquinolyl)carbamoyloxy)hexyl (2S)-2-amino-3- methylbutanoate 586.3 (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 6-(N-(3-isoquinolyl)carbamoyloxy)hexyl (2R)-2-amino-3- methylbutanoate 764.1 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl (2S)-3-(tert-butoxy)-2-[(tert- butoxy)carbonylamino]propanoate 608.1 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl (2S)-2-amino-3-hydroxypropanoate 764.1 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl (2R)-3-(tert-butoxy)-2-[(tert- butoxy)carbonylamino]propanoate 608.1 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexyl (2R)-2-amino-3-hydroxypropanoate 532.1 methyl (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-pyridino[4,3-d]pyridin-3- ylcarbamoyloxy)hexanoate 518.1 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-pyridino[4,3-d]pyridin-3- ylcarbamoyloxy)hexanoic acid 504.1 N-{(1S)-5-hydroxy-1-[(N-pyridino[4,3-d]pyridin-3- ylcarbamoyloxy)methyl]pentyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 532.1 methyl (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-pyridino[3,4-d]pyridin-3- ylcarbamoyloxy)hexanoate 518.1 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-pyridino[3,4-d]pyridin-3- ylcarbamoyloxy)hexanoic acid 489.2 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-3,4- dihydroxybutyl){[(3-fluorophenyl)methyl]amino}-N-methylcarboxamide 489.1 methyl 3-{[2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]carbonylamino}isoquinoline-7-carboxylate 568.2 N-((1S)-5-diazo-3,3-difluoro-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-5-azapent-5-enyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 472.2 [(2S)-5-amino-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)pentyloxy]-N-(5-chloro(2-pyridyl))carboxamide 444.2 [(2S)-3-amino-2-({[(3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-(6-fluoro(3-isoquinolyl))carboxamide 472.1 N-{(1S)-1-[(N-pyridino[3,4-d]pyridin-3-ylcarbamoyloxy)methyl]but-3- enyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide 506.1 N-{(1S)-3,4-dihydroxy-1-[(N-pyridino[3,4-d]pyridin-3- ylcarbamoyloxy)methyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 542.2 N-((1S)-4-amino-3,3-difluoro-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 622.2 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl (2S)-2-amino-3-methylbutanoate 622.2 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl (2R)-2-amino-3-methylbutanoate 610.1 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl (2S)-2-amino-3-hydroxypropanoate 610.1 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl (2R)-2-amino-3-hydroxypropanoate 686.2 N-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]propyl][4- (phenylcarbonyl)phenyl]carboxamide 686.2 N-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]propyl][3- (phenylcarbonyl)phenyl]carboxamide 696.1 N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)pentyl][4- (phenylcarbonyl)phenyl]carboxamide 696.2 N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)pentyl][3- (phenylcarbonyl)phenyl]carboxamide 612.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[(phenylmethoxy)carbonylamino]propoxy]-N- (6-fluoro(3-isoquinolyl))carboxamide 635.2 N-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]propyl]-2-[(tert- butoxy)carbonylamino]acetamide 461.0 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-(2-{N-[7- (hydroxymethyl)(3-isoquinolyl)]carbamoyloxy}ethyl)-N- methylcarboxamide 461.1 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-(2-{N-[6- (hydroxymethyl)(3-isoquinolyl)]carbamoyloxy}ethyl)-N- methylcarboxamide 471.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)pent-4-enyloxy]-N-(3-isoquinolyl)carboxamide 509.1 {[(5-bromo-2-chlorophenyl)methyl]amino}-N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-N-methylcarboxamide 457.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)pent-4-enyloxy]-N-(5-chloro(2- pyridyl))carboxamide 505.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(3- isoquinolyl)carboxamide 489.2 methyl 4-chloro-3-{[(N-{2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}-N- methylcarbamoyl)amino]methyl}benzoate 505.2 [(2S,4R)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(3- isoquinolyl)carboxamide 505.2 [(2S,4S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(3- isoquinolyl)carboxamide 489.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(5-chloro(2- pyridyl))carboxamide 585.2 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl dihydrogen phosphate 490.2 [(2S)-2-({[(3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-4,5- dihydroxypentyloxy]-N-(3-isoquinolyl)carboxamide 565.2 (5S)-5-({[(2-chlorophenyl)methyl]amino}-N-methylcarbonylamino)-6- (N-(3-isoquinolyl)carbamoyloxy)hexyl dihydrogen phosphate 590.2 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl 2-(dimethylamino)acetate 619.1 N-{(1S)-4-(1,3-dioxobenzo[c]azolin-2-yl)-1-[(N-pyridino[3,4-d]pyridin- 3-ylcarbamoyloxy)methyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 489.1 N-{(1S)-4-amino-1-[(N-pyridino[3,4-d]pyridin-3- ylcarbamoyloxy)methyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 489.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-hydroxypentyloxy]-N-(3- isoquinolyl)carboxamide 569.2 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)pentyl dihydrogen phosphate 571.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-oxo-5-piperazinylpentyloxy]-N-(3- isoquinolyl)carboxamide 672.2 tert-butyl 4-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoyl]piperazinecarboxylate 455.2 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]but-3-enyl}{[(2,3- difluorophenyl)methyl]amino}-N-methylcarboxamide 489.2 N-{(1S)-3,4-dihydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2,3- difluorophenyl)methyl]amino}-N-methylcarboxamide 489.2 N-{(1S,3S)-3,4-dihydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2,3- difluorophenyl)methyl]amino}-N-methylcarboxamide 489.2 N-{(1S,3R)-3,4-dihydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2,3- difluorophenyl)methyl]amino}-N-methylcarboxamide 461.2 ({[2-chloro-5-(hydroxymethyl)phenyl]methyl}amino)-N-{2-[N-(6- fluoro(3-isoquinolyl))carbamoyloxy]ethyl}-N-methylcarboxamide 569.2 (4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 2-hydroxy-5-(N-(3-isoquinolyl)carbamoyloxy)pentyl dihydrogen phosphate 501.2 N-[(2S)-2-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3-isoquinolyl)carbamoyloxy)propyl]-2- aminoacetamide 508.1 N-{(1S)-4-amino-3,3-difluoro-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2,3- difluorophenyl)methyl]amino}-N-methylcarboxamide 524.2 N-{(1S)-4-amino-3,3-difluoro-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 603.2 (4S,2R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl dihydrogen phosphate 603.2 (2S,4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl dihydrogen phosphate 639.1 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3-isoquinolyl)carbamoyloxy)hexyl diethyl phosphate 472.2 N-{(1S)-1-[(N-pyridino[4,3-d]pyridin-3-ylcarbamoyloxy)methyl]but-3- enyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide 506.2 N-{(1S)-3,4-dihydroxy-1-[(N-pyridino[4,3-d]pyridin-3- ylcarbamoyloxy)methyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 517.1 N-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3-isoquinolyl)carbamoyloxy)propyl]-2- aminoacetamide 611.2 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3-isoquinolyl)carbamoyloxy)hexyl dimethyl phosphate 583.2 (5S)-5-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3-isoquinolyl)carbamoyloxy)hexyl dihydrogen phosphate 533.2 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]hexanoate 569.2 (4S,2R)-4-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl dihydrogen phosphate 569.2 (2S,4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl dihydrogen phosphate 505.2 [(2S)-2-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 6-hydroxyhexyloxy]-N-(6-fluoro(3-isoquinolyl))carboxamide 613.1 (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 6-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]hexyl dimethyl phosphate 585.1 (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 6-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]hexyl dihydrogen phosphate 541.2 [(2S)-2-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 4-oxo-4-piperazinylbutoxy]-N-(3-isoquinolyl)carboxamide 557.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-oxo-4-piperazinylbutoxy]-N-(3- isoquinolyl)carboxamide 507.2 [(2S,4S)-2-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 507.2 [(2S,4R)-2-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 531.1 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(5-phenylisoxazol-3- yl)carbamoyloxy]hexanoate 515.2 methyl (5R)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3-isoquinolyl)carbamoyloxy)hexanoate 499.1 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(5-chloro(2- pyridyl))carbamoyloxy]hexanoate 490.5 N-{(1S)-3,4-dihydroxy-1-[(N-quinazolin-2- ylcarbamoyloxy)methyl]butyl}{[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 511.1 [(2S,4R)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-benzothiazol-2- ylcarboxamide 501.2 methyl (4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)pentanoate 519.2 methyl (4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanoate 473.2 N-{(1S)-4-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2,3- difluorophenyl)methyl]amino}-N-methylcarboxamide 491.2 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-4- hydroxybutyl){[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 548.5 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(5-phenyl(1,3,4-thiadiazol-2- yl))carbamoyloxy]hexanoate 566.5 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4-fluorophenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate 582.5 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4-chlorophenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate 562.5 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4-methylphenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate 578.5 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4-methoxyphenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate 582.5 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(2-chlorophenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate 487.2 [(2R)-2-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 6-hydroxyhexyloxy]-N-(3-isoquinolyl)carboxamide 595.2 (5R)-5-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 6-(N-(3-isoquinolyl)carbamoyloxy)hexyl dimethyl phosphate 567.5 (5R)-5-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 6-(N-(3-isoquinolyl)carbamoyloxy)hexyl dihydrogen phosphate 583.5 (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 6-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]hexyl hydroxysulfonate 523.5 [(2R,4R)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 549.4 [(2R)-3-((4R)-2-oxo(1,3-dioxolan-4-yl))-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)propoxy]-N-(6- fluoro(3-isoquinolyl))carboxamide 559.2 [(2S)-2-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 4-oxo-4-piperazinylbutoxy]-N-(6-fluoro(3-isoquinolyl))carboxamide 571.5 (4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]pentyl dihydrogen phosphate 487.4 (4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 5-(N-(3-isoquinolyl)carbamoyloxy)pentanoic acid 505.5 (4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]pentanoic acid 655.7 tert-butyl 4-[(4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoyl]piperazinecarboxylate 673.7 tert-butyl 4-[(4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentanoyl]piperazinecarboxylate 533.1 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(trifluoromethyl)(2- pyridyl)]carbamoyloxy}hexanoate 627.5 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4-bromophenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate 573.5 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4-cyanophenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate 566.5 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(2-fluorophenyl)(1,3,4-thiadiazol-2- yl)]carbamoyloxy}hexanoate 553.4 (4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 5-(N-(3-isoquinolyl)carbamoyloxy)pentyl dihydrogen phosphate 601.5 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl hydroxysulfonate 503.1 N-((1S)-5-hydroxy-1-{[N-(5-phenylisoxazol-3- yl)carbamoyloxy]methyl}pentyl){[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 603.1 (2S,4R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl dihydrogen phosphate 603.1 (2R,4R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl dihydrogen phosphate 523.2 N-((3S,1R)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-3,4- dihydroxybutyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 549.2 N-{(1R)-1-[((4S)-2-oxo(1,3-dioxolan-4-yl))methyl]-2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 555.4 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-oxo-4- piperazinylbutyl}{[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 573.4 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-4-oxo-4- piperazinylbutyl){[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 511.2 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(tert-butyl)isoxazol-3- yl]carbamoyloxy}hexanoate 587.2 (4S,2R)-4-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl dihydrogen phosphate 495.1 ({(1S,3R)-1-[(N-benzoxazol-2-ylcarbamoyloxy)methyl]-3,4- dihydroxybutyl}methylamino)-N-[(2-chloro-3- fluorophenyl)methyl]carboxamide 529.1 [((1S,3R)-1-{[N-(5-chlorobenzoxazol-2-yl)carbamoyloxy]methyl}-3,4- dihydroxybutyl)methylamino]-N-[(2-chloro-3- fluorophenyl)methyl]carboxamide 545.1 methyl (5S)-5-({N-[(2,3- difluorophenyl)methyl]carbamoyl}methylamino)-6-{N-[5-(4- methylphenyl)isoxazol-3-yl]carbamoyloxy}hexanoate 561.1 N-{1-[((4R)-2,2-dimethyl(1,3-dioxolan-4-yl))methyl](1S)-2-[N-(5- phenylisoxazol-3-yl)carbamoyloxy]ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 521.1 N-((1S,3R)-3,4-dihydroxy-1-{[N-(5-phenylisoxazol-3- yl)carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 523.1 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(trifluoromethyl)isoxazol-3- yl]carbamoyloxy}hexanoate 625.2 (2S,4R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl diethyl phosphate 625.2 (2R,4R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2- hydroxypentyl diethyl phosphate 761.7 (3S,1R)-3-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-1-[(ethoxyphosphinyl)methyl]-4-(N-(3- isoquinolyl)carbamoyloxy)butyl diethyl phosphate 625.6 (4S,2R)-4-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl diethyl phosphate 537.1 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-4- hydroxy-3-(hydroxymethyl)butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 549.1 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4-fluorophenyl)isoxazol-3- yl]carbamoyloxy}hexanoate 609.1 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-{N-[5-(4-bromophenyl)isoxazol-3- yl]carbamoyloxy}hexanoate 521.1 N-[(1S)-1-({N-[5-(4-fluorophenyl)isoxazol-3-yl]carbamoyloxy}methyl)- 5-hydroxypentyl]{[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 581.1 N-[(1S)-1-({N-[3-(4-bromophenyl)isoxazol-5-yl]carbamoyloxy}methyl)- 5-hydroxypentyl]{[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 528.1 N-[(1S)-1-({N-[3-(4-cyanophenyl)isoxazol-5-yl]carbamoyloxy}methyl)- 5-hydroxypentyl]{[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 531.1 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(3-phenylisoxazol-5- yl)carbamoyloxy]hexanoate 503.1 N-((1S)-5-hydroxy-1-{[N-(3-phenylisoxazol-5- yl)carbamoyloxy]methyl}pentyl){[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 685.6 [(2S)-5-({[(tert-butoxy)carbonylamino]sulfonyl}amino)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)pentyloxy]-N-(6- fluoro(3-isoquinolyl))carboxamide 585.5 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-4- (sulfamoylamino)butyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 564.5 N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]-2-hydroxyacetamide 594.0 N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]-2,3-dihydroxypropanamide 613.5 N-((1S)-4-{[(dimethylamino)sulfonyl]amino}-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 612.5 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-4- [(propylsulfonyl)amino]butyl){[(2-chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide 543.5 N-((1S)-3,3-difluoro-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}-4-hydroxybutyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 583.2 (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 6-[N-(5-phenylisoxazol-3-yl)carbamoyloxy]hexyl dihydrogen phosphate 539.5 [(2S,4R)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(5,6- dimethylbenzothiazol-2-yl)carboxamide 617.6 N-[4-({(1E)-2-cyano-1-[(2-hydroxyethyl)amino]-2-azavinyl}amino)(1S)- 1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}butyl]{[(2-chloro- 3-fluorophenyl)methyl]amino}-N-methylcarboxamide 591.4 (4S,2R)-5-(N-benzothiazol-2-ylcarbamoyloxy)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-2-hydroxypentyl dihydrogen phosphate 599.6 N-[4-({(1E)-2-cyano-1-[(2-hydroxyethyl)amino]-2-azavinyl}amino)(1S)- 1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]butyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 613.6 N-[4-({(1E)-2-cyano-1-[(3-hydroxypropyl)amino]-2- azavinyl}amino)(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 525.4 [(2S,4R)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(6- methylbenzothiazol-2-yl)carboxamide 629.6 N-{4-[((1E)-2-cyano-1-{[2-hydroxy-1-(hydroxymethyl)ethyl]amino}-2- azavinyl)amino](1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 651.5 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2,2-difluoro-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl dimethyl phosphate 672.6 {N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]carbamoyl}methyl dimethyl phosphate 623.5 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2,2-difluoro-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl dihydrogen phosphate 657.6 (4S,2R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-[N-(5-phenylisoxazol-3- yl)carbamoyloxy]pentyl diethyl phosphate 599.4 (4S,2R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-[N-(5-phenylisoxazol-3- yl)carbamoyloxy]pentyl dihydrogen phosphate 546.4 [(2S,4R)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(6- chlorobenzothiazol-2-yl)carboxamide 529.4 [(2S,4R)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(6- fluorobenzothiazol-2-yl)carboxamide 547.4 [(2S,4R)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(5,6- difluorobenzothiazol-2-yl)carboxamide 535.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-hydroxy-4,4-dimethylpentyloxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 615.5 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-2,2- dimethylpentyl dihydrogen phosphate 537.2 N-[(1S)-1-({N-[5-(4-chlorophenyl)isoxazol-3-yl]carbamoyloxy}methyl)- 5-hydroxypentyl]{[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 537.2 N-[(1S)-1-({N-[5-(2-chlorophenyl)isoxazol-3-yl]carbamoyloxy}methyl)- 5-hydroxypentyl]{[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 521.1 N-[(1S)-1-({N-[5-(3-fluorophenyl)isoxazol-3-yl]carbamoyloxy}methyl)- 5-hydroxypentyl]{[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 561.1 N-{1-[((4R)-2,2-dimethyl(1,3-dioxolan-4-yl))methyl](1S)-2-[N-(3- phenylisoxazol-5-yl)carbamoyloxy]ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 521.1 N-((1S,3R)-3,4-dihydroxy-1-{[N-(3-phenylisoxazol-5- yl)carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 544.2 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(1-methyl-5-phenylpyrazol-3- yl)carbamoyloxy]hexanoate 544.2 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(1-methyl-3-phenylpyrazol-5- yl)carbamoyloxy]hexanoate 516.2 N-((1S)-5-hydroxy-1-{[N-(1-methyl-5-phenylpyrazol-3- yl)carbamoyloxy]methyl}pentyl){[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 516.2 N-((1S)-5-hydroxy-1-{[N-(1-methyl-3-phenylpyrazol-5- yl)carbamoyloxy]methyl}pentyl){[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 562.1 N-{1-[((4R)-2,2-dimethyl(1,3-dioxolan-4-yl))methyl](1S)-2-[N-(5- phenyl(1,2,4-oxadiazol-3-yl))carbamoyloxy]ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 522.4 N-((1S,3R)-3,4-dihydroxy-1-{[N-(5-phenyl(1,2,4-oxadiazol-3- yl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 635.6 ethyl 2-({N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]carbamoyl}amino)acetate 537.2 N-[(1S)-1-({N-[5-(3-chlorophenyl)isoxazol-3-yl]carbamoyloxy}methyl)- 5-hydroxypentyl]{[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 545.1 methyl (5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-[N-(4-methyl-3-phenylisoxazol-5- yl)carbamoyloxy]hexanoate 697.6 2-[((1E)-1-{[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl]amino}-2-carbamoyl-2- azavinyl)amino]ethyl dihydrogen phosphate 593.6 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-{[(2- hydroxyethyl)amino]carbonylamino}pentyloxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 545.1 N-{1-[((4R)-2,2-dimethyl(1,3-dioxolan-4-yl))methyl](1S)-2-[N-(5- phenylisoxazol-3-yl)carbamoyloxy]ethyl}{[(2,3- difluorophenyl)methyl]amino}-N-methylcarboxamide 505.1 N-((1S,3R)-3,4-dihydroxy-1-{[N-(5-phenylisoxazol-3- yl)carbamoyloxy]methyl}butyl){[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 641.6 (4S,2R)-4-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-[N-(5-phenylisoxazol-3- yl)carbamoyloxy]pentyl diethyl phosphate 777.2 (3S,1R)-3-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-1-[(ethoxyphosphinyl)methyl]-4-[N-(5- phenylisoxazol-3-yl)carbamoyloxy]butyl diethyl phosphate 585.5 (4S,2R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl dihydrogen phosphate 583.5 (4S,2R)-4-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-[N-(5-phenylisoxazol-3- yl)carbamoyloxy]pentyl dihydrogen phosphate 673.6 2-({N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]carbamoyl}amino)ethyl dihydrogen phosphate 539.1 N-[(1S,3R)-1-({N-[5-(3-fluorophenyl)isoxazol-3- yl]carbamoyloxy}methyl)-3,4-dihydroxybutyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 579.1 N-(1-[((4R)-2,2-dimethyl(1,3-dioxolan-4-yl))methyl](1S)-2-{N-[5-(3- fluorophenyl)isoxazol-3-yl]carbamoyloxy}ethyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 523.2 N-{(1S)-2-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-1-[(2- hydroxyethoxy)methyl]ethyl}{[(2-chloro-3-fluorophenyl)methyl]amino}- N-methylcarboxamide 603.2 2-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]propoxy]ethyl dihydrogen phosphate 607.1 N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl][(3-hydroxypropyl)amino]carboxamide 625.5 (4S,2R)-5-[N-(6-chlorobenzothiazol-2-yl)carbamoyloxy]-4-({[(2-chloro- 3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)-2- hydroxypentyl dihydrogen phosphate 617.6 N-[4-({(1E)-2-carbamoyl-1-[(2-hydroxyethyl)amino]-2- azavinyl}amino)(1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 635.6 N-[4-({(1E)-2-carbamoyl-1-[(2-hydroxyethyl)amino]-2- azavinyl}amino)(1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 659.7 N-[4-({(1E)-2-cyano-1-[(3-hydroxy-2,2-dimethylpropyl)amino]-2- azavinyl}amino)(1S)-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 631.5 2-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]propoxy]ethyl dimethyl phosphate 675.1 (4S,2R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-{N-[5-(3-fluorophenyl)isoxazol-3- yl]carbamoyloxy}-2-hydroxypentyl diethyl phosphate 617.5 (4S,2R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-{N-[5-(3-fluorophenyl)isoxazol-3- yl]carbamoyloxy}-2-hydroxypentyl dihydrogen phosphate 609.4 (4S,2R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluorobenzothiazol-2-yl)carbamoyloxy]- 2-hydroxypentyl dihydrogen phosphate 743.7 3-({N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]carbamoyl}amino)-2,2-dimethylpropyl dimethyl phosphate 715.7 3-({N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl]carbamoyl}amino)-2,2-dimethylpropyl dihydrogen phosphate 601.5 (4S,2R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-[N-(3-phenylisoxazol-5- yl)carbamoyloxy]pentyl dihydrogen phosphate 565.6 N-{(1S)-2-[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]-1-[(3-hydroxy-2,2- dimethylpropoxy)methyl]ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 647.6 N-[4-({(1E)-2-cyano-1-[(3-hydroxy-2,2-dimethylpropyl)amino]-2- azavinyl}amino)(1S)-1-[(N-benzothiazol-2- ylcarbamoyloxy)methyl]butyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 605.5 N-[4-({(1E)-2-cyano-1-[(2-hydroxyethyl)amino]-2-azavinyl}amino)(1S)- 1-[(N-benzothiazol-2-ylcarbamoyloxy)methyl]butyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 529.5 N-{1-[((4R)-2,2-dimethyl(1,3-dioxolan-4-yl))methyl](1S)-2-(N-(3- isoquinolyl)carbamoyloxy)ethyl}{[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 595.1 N-(1-[((4R)-2,2-dimethyl(1,3-dioxolan-4-yl))methyl](1S)-2-{N-[5-(3- chlorophenyl)isoxazol-3-yl]carbamoyloxy}ethyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 555.5 N-[(1S,3R)-1-({N-[5-(3-chlorophenyl)isoxazol-3- yl]carbamoyloxy}methyl)-3,4-dihydroxybutyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 643.5 3-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]propoxy]-2,2-dimethylpropyl dihydrogen phosphate 635.5 (4S,2R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-{N-[5-(3-chlorophenyl)isoxazol-3- yl]carbamoyloxy}-2-hydroxypentyl dihydrogen phosphate 472.5 N-{(1S)-4-amino-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2,3- difluorophenyl)methyl]amino}-N-methylcarboxamide 490.5 N-((1S)-4-amino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2,3- difluorophenyl)methyl]amino}-N-methylcarboxamide 603.6 N-{1-[({(1E)-2-cyano-1-[(3-hydroxypropyl)amino]-2- azavinyl}amino)methyl](1S)-2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 504.5 N-{(1S)-1-[(N-benzothiazol-2-ylcarbamoyloxy)methyl]-5-diazo-5- azapent-5-enyl}{[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 478.1 N-{(1S)-4-amino-1-[(N-benzothiazol-2- ylcarbamoyloxy)methyl]butyl}{[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 516.5 N-((1S)-5-diazo-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}- 5-azapent-5-enyl){[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 626.5 2-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoylamino]ethyl dihydrogen phosphate 668.6 3-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoylamino]-2,2-dimethylpropyl dihydrogen phosphate 587.2 3-{[(5S)-5-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-6-(N-(3- isoquinolyl)carbamoyloxy)hexyl]oxycarbonyl}propanoic acid 546.0 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-N-(2-hydroxyethyl)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanamide 635.2 N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl][(3-hydroxy-2,2- dimethylpropyl)amino]carboxamide 560.0 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-N-(3-hydroxypropyl)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanamide 588.0 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-N-(3-hydroxy-2,2-dimethylpropyl)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanamide 560.0 (4S)-N-((2S)-2-hydroxypropyl)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanamide 560.0 N-((2R)-2-hydroxypropyl)(4S)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanamide 553.1 N-{(1S)-1-[((2S)-2,3-dihydroxypropoxy)methyl]-2-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 738.6 2-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoylamino]ethyl ditert-butyl phosphate 615.7 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[4-(2-hydroxyethyl)piperazinyl]-5- oxopentyloxy]-N-(3-isoquinolyl)carboxamide 504.2 N-((1S)-3-carbamoyl-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}propyl){[(2,3- difluorophenyl)methyl]amino}-N-methylcarboxamide 504.5 N-((1S)-4-amino-1-{[N-(3-phenylisoxazol-5- yl)carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 523.5 methyl (4S)-5-(N-benzothiazol-2-ylcarbamoyloxy)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)pentanoate 699.5 tert-butyl 4-[(4S)-5-(N-benzothiazol-2-ylcarbamoyloxy)-4-({[(2-chloro-3- M + Na⁺ fluorophenyl)methyl]amino}-N- methylcarbonylamino)pentanoyl]piperazinecarboxylate 687.2 tert-butyl 4-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3-phenylisoxazol-5- yl)carbamoyloxy]pentanoyl]piperazinecarboxylate 587.2 N-((1S)-4-oxo-1-{[N-(3-phenylisoxazol-5-yl)carbamoyloxy]methyl}-4- piperazinylbutyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 577.1 N-{(1S)-1-[(N-benzothiazol-2-ylcarbamoyloxy)methyl]-4-oxo-4- piperazinylbutyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 687.2 tert-butyl 4-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(5-phenylisoxazol-3- yl)carbamoyloxy]pentanoyl]piperazinecarboxylate 587.2 N-((1S)-4-oxo-1-{[N-(5-phenylisoxazol-3-yl)carbamoyloxy]methyl}-4- piperazinylbutyl){[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 695.7 2-{4-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoyl]piperazinyl}ethyl dihydrogen phosphate 723.7 2-{4-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoyl]piperazinyl}ethyl dimethyl phosphate 633.6 ethyl 2-({N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3-phenylisoxazol-5- yl)carbamoyloxy]pentyl]carbamoyl}amino)acetate 507.4 (4S)-5-(N-benzothiazol-2-ylcarbamoyloxy)-4-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)pentanoic acid 591.6 N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3-phenylisoxazol-5- yl)carbamoyloxy]pentyl][(2-hydroxyethyl)amino]carboxamide 535.1 N-{(1S)-1-[((2S)-2,3-dihydroxypropoxy)methyl]-2-(N-(3- isoquinolyl)carbamoyloxy)ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 517.1 methyl (4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(5-phenylisoxazol-3- yl)carbamoyloxy]pentanoate 517.1 methyl (4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3-phenylisoxazol-5- yl)carbamoyloxy]pentanoate 699.6 2-({N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3-phenylisoxazol-5- yl)carbamoyloxy]pentyl]carbamoyl}amino)ethyl dimethyl phosphate 669.5 2-({N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3-phenylisoxazol-5- yl)carbamoyloxy]pentyl]carbamoyl}amino)ethyl dihydrogen phosphate 617.6 ethyl 2-({N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl]carbamoyl}amino)acetate 671.2 tert-butyl 4-[(4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(5-phenylisoxazol-3- yl)carbamoyloxy]pentanoyl]piperazinecarboxylate 571.2 [(2S)-2-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 5-oxo-5-piperazinylpentyloxy]-N-(5-phenylisoxazol-3-yl)carboxamide 671.2 tert-butyl 4-[(4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3-phenylisoxazol-5- yl)carbamoyloxy]pentanoyl]piperazinecarboxylate 571.2 [(2S)-2-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 5-oxo-5-piperazinylpentyloxy]-N-(3-phenylisoxazol-5-yl)carboxamide 505.2 N-{(1S)-1-[(2-hydroxyethoxy)methyl]-2-(N-(3- isoquinolyl)carbamoyloxy)ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 585.2 2-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3-isoquinolyl)carbamoyloxy)propoxy]ethyl dihydrogen phosphate 597.1 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)-2,2- dimethylpentyl dihydrogen phosphate 517.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-hydroxy-4,4-dimethylpentyloxy]-N-(3- isoquinolyl)carboxamide 613.5 (2R)-3-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3-isoquinolyl)carbamoyloxy)propoxy]-2- hydroxypropyl dihydrogen phosphate 683.7 2-({N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl]carbamoyl}amino)ethyl dimethyl phosphate 575.6 N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)pentyl][(2- hydroxyethyl)amino]carboxamide 655.5 2-({N-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl]carbamoyl}amino)ethyl dihydrogen phosphate 533.1 methyl (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3-phenylisoxazol-5- yl)carbamoyloxy]pentanoate 701.2 tert-butyl 4-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[N-(3-phenylisoxazol-5- yl)carbamoyloxy]pentanoyl]-1,4-diazaperhydroepinecarboxylate 601.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(1,4-diazaperhydroepinyl)-5-oxopentyloxy]-N- (3-phenylisoxazol-5-yl)carboxamide 601.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(4-methylpiperazinyl)-5-oxopentyloxy]-N-(3- phenylisoxazol-5-yl)carboxamide 533.1 N-((1S)-4-hydroxy-3,3-dimethyl-1-{[N-(3-phenylisoxazol-5- yl)carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 629.2 methyl 4-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3- isoquinolyl)carbamoyloxy)pentanoyl]piperazine-2-carboxylate 601.1 N-{(1S)-4-[3-(hydroxymethyl)piperazinyl]-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-4-oxobutyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 701.2 tert-butyl 4-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)pentanoyl]-2- (hydroxymethyl)piperazinecarboxylate 641.2 (4S,2R)-4-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-[N-(3-phenylisoxazol-5- yl)carbamoyloxy]pentyl diethyl phosphate 601.2 N-{(1S)-4-[(3S)-3-(hydroxymethyl)piperazinyl]-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-4-oxobutyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 665.3 (4S)-4-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 5-(N-(3-isoquinolyl)carbamoyloxy)pentyl ditert-butyl phosphate 533.5 N-((1S)-4-hydroxy-4-methyl-1-{[N-(3-phenylisoxazol-5- yl)carbamoyloxy]methyl}pentyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 535.5 N-{1-[((2R)-2,3-dihydroxypropoxy)methyl](1S)-2-(N-(3- isoquinolyl)carbamoyloxy)ethyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 595.2 N-{1-[((2R)-2,3-dihydroxypropoxy)methyl](1S)-2-(N-(3- isoquinolyl)carbamoyloxy)ethyl}-N-((2S)-2,3-dihydroxypropyl){[(2- chloro-3-fluorophenyl)methyl]amino}carboxamide 601.2 N-{4-[(3R)-3-(hydroxymethyl)piperazinyl](1S)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-4-oxobutyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 615.5 (2S)-3-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3-isoquinolyl)carbamoyloxy)propoxy]-2- hydroxypropyl dihydrogen phosphate 599.6 (2S)-3-[(2S)-2-({[(2,3-difluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3-isoquinolyl)carbamoyloxy)propoxy]-2- hydroxypropyl dihydrogen phosphate 519.2 N-{(1S)-1-[((2S)-2,3-dihydroxypropoxy)methyl]-2-(N-(3- isoquinolyl)carbamoyloxy)ethyl}{[(2,3-difluorophenyl)methyl]amino}-N- methylcarboxamide 505.2 [(2R,4R)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(3- isoquinolyl)carboxamide 505.2 [(4S,2R)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,5-dihydroxypentyloxy]-N-(3- isoquinolyl)carboxamide 585.5 (2S,4R)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2-hydroxy-5-(N-(3- isoquinolyl)carbamoyloxy)pentyl dihydrogen phosphate 608.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-imidazo[2,1-c]piperazin-7-yl-5-oxopentyloxy]- N-(3-isoquinolyl)carboxamide 571.6 [(2R)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-oxo-5-piperazinylpentyloxy]-N-(3- isoquinolyl)carboxamide 610.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-oxo-5-(1,2,4-triazolo[3,4-c]piperazin-7- yl)pentyloxy]-N-(3-isoquinolyl)carboxamide 642.6 N-((1S)-4-[(tert-butoxy)carbonylamino]-3,3-difluoro-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 570.5 N-((1S)-4-carbonylamino-3,3-difluoro-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 527.2 [(2S)-2-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 4-imidazol-2-ylbutoxy]-N-(6-fluoro(3-isoquinolyl))carboxamide 618.6 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-4- (piperazinylcarbonylamino)butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 571.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4,4-difluoro-5-hydroxy-5-methylhexyloxy]-N-(6- fluoro(3-isoquinolyl))carboxamide 594.6 N-{(1S)-4-imidazo[5,1-c]piperazin-7-yl-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 595.2 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-(1,2,4- triazolo[3,4-c]piperazin-7-yl)butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 692.1 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2,2-difluoro-5-[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]pentyl 4-nitrobenzoate 708.1 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-2,2-difluoro-5-{N-[5-(3-fluorophenyl)isoxazol-3- yl]carbamoyloxy}pentyl 4-nitrobenzoate 559.1 N-[(1S)-3,3-difluoro-1-({N-[5-(3-fluorophenyl)isoxazol-3- yl]carbamoyloxy}methyl)-4-hydroxybutyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 534.1 N-((1S)-4-carbonylamino-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 578.1 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-4-[(2- hydroxy-2-methylpropyl)amino]butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 650.2 N-((1S)-4-[bis(2-hydroxy-2-methylpropyl)amino]-1-{[N-(6-fluoro(3- isoquinolyl))carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 542.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[(2,2,2-trifluoroethyl)amino]propoxy]-N-(3- isoquinolyl)carboxamide 524.2 [(2S)-3-[(2,2-difluoroethyl)amino]-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)propoxy]-N-(3- isoquinolyl)carboxamide 532.2 methyl 2-{[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3- isoquinolyl)carbamoyloxy)propyl]amino}acetate 532.3 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[(2-hydroxy-2-methylpropyl)amino]propoxy]- N-(3-isoquinolyl)carboxamide 571.5 N-((1S)-1-{[N-(6-fluoro(3-isoquinolyl))carbamoyloxy]methyl}-3- hydroxy-3-methylbutyl)-N-(2,2-difluoroethyl){[(2-chloro-3- fluorophenyl)methyl]amino}carboxamide 541.1 N-((1S)-3,3-difluoro-4-hydroxy-1-{[N-(5-phenylisoxazol-3- yl)carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 541.1 N-((1S)-3,3-difluoro-4-hydroxy-1-{[N-(3-phenylisoxazol-5- yl)carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 525.1 N-{(1S)-3,3-difluoro-4-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 537.1 N-[(1S)-1-({N-[5-(3-fluorophenyl)isoxazol-3-yl]carbamoyloxy}methyl)- 3-hydroxy-3-methylbutyl]{[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 519.1 N-((1S)-3-hydroxy-3-methyl-1-{[N-(5-phenylisoxazol-3- yl)carbamoyloxy]methyl}butyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 515.2 (4R)-4-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 5-(N-(3-isoquinolyl)carbamoyloxy)pentyl acetate 473.5 N-{(1R)-4-hydroxy-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2,3- difluorophenyl)methyl]amino}-N-methylcarboxamide 553.5 (4R)-4-({[(2,3-difluorophenyl)methyl]amino}-N-methylcarbonylamino)- 5-(N-(3-isoquinolyl)carbamoyloxy)pentyl dihydrogen phosphate 506.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[(2-fluoroethyl)amino]propoxy]-N-(3- isoquinolyl)carboxamide 553.5 N-{(1S)-3-hydroxy-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-3- methylbutyl}-N-(2,2-difluoroethyl){[(2-chloro-3- fluorophenyl)methyl]amino}carboxamide 587.5 N-[(1S)-1-({N-[5-(3-fluorophenyl)isoxazol-3-yl]carbamoyloxy}methyl)- 3-hydroxy-3-methylbutyl]-N-(2,2-difluoroethyl){[(2-chloro-3- fluorophenyl)methyl]amino}carboxamide 599.1 N-[(1S)-3,3-difluoro-1-({N-[3-(3-fluorophenyl)isoxazol-5- yl]carbamoyloxy}methyl)-4-hydroxybutyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 551.5 methyl (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-{N-[3-(3-fluorophenyl)isoxazol-5- yl]carbamoyloxy}pentanoate 543.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(1-methylimidazol-4-yl)propoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 538.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[(methylsulfonyl)amino]propoxy]-N-(3- isoquinolyl)carboxamide 529.5 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-imidazol-4-ylpropoxy]-N-(6-fluoro(3- isoquinolyl))carboxamide 663.2 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-[2- (trifluoromethyl)(1,2,4-triazolo[5,1-c]piperazin-7-yl)]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 522.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(2-pyridyl)propoxy]-N-(3- isoquinolyl)carboxamide 605.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-oxo-5-piperazinylpentyloxy]-N-[3-(3- fluorophenyl)isoxazol-5-yl]carboxamide 605.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-oxo-5-piperazinylpentyloxy]-N-[5-(3- fluorophenyl)isoxazol-3-yl]carboxamide 705.1 tert-butyl 4-[(4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-{N-[3-(3-fluorophenyl)isoxazol-5- yl]carbamoyloxy}pentanoyl]piperazinecarboxylate 580.1 N-{(1S)-3-imidazo[1,5-a]piperazin-3-yl-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]propyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 580.1 [(2S)-4-(7-{N-[(2-chloro-3-fluorophenyl)methyl]carbamoyl}imidazo[1,5- a]piperazin-3-yl)-2-(methylamino)butoxy]-N-(3-isoquinolyl)carboxamide 765.1 N-[(1S)-3-(7-{N-[(2-chloro-3- fluorophenyl)methyl]carbamoyl}imidazo[1,5-a]piperazin-3-yl)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]propyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 680.2 tert-butyl 3-[(3S)-3-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-(N-(3- isoquinolyl)carbamoyloxy)butyl]imidazo[5,1-c]piperazine-7-carboxylate 594.1 (4S)-4-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(N-(3-isoquinolyl)carbamoyloxy)-N-(pyrazin-2- ylmethyl)pentanamide 576.1 N-{(1S)-3-(4-hydroimidazo[1,5-a]pyrazin-3-yl)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]propyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 613.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[4-(methylethyl)piperazinyl]-5-oxopentyloxy]- N-(3-isoquinolyl)carboxamide 627.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(9-oxa-3,6-diazabicyclo[4.4.0]dec-3-yl)-5- oxopentyloxy]-N-(3-isoquinolyl)carboxamide 585.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(4-methylpiperazinyl)-5-oxopentyloxy]-N-(3- isoquinolyl)carboxamide 595.1 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-(1,2,4- triazolo[5,1-c]piperazin-7-yl)butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 609.1 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-(3-methyl(1,2,4- triazolo[3,4-c]piperazin-7-yl))butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 606.1 N-{(1S)-4-(1,1-dioxo(1,4-thiazaperhydroin-4-yl))-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 571.1 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-(4- methylpiperazinyl)butyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 558.1 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-morpholin-4- ylbutyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 557.1 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4- piperazinylbutyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 601.2 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-(2-(N-(3- isoquinolyl)carbamoyloxy)-1-{[1-benzylimidazol-2-yl]methyl}ethyl)-N- methylcarboxamide 525.2 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-{2-(N-(3- isoquinolyl)carbamoyloxy)-1-[(1-methylimidazol-2-yl)methyl]ethyl}-N- methylcarboxamide 511.1 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-[1-(imidazol-2-ylmethyl)- 2-(N-(3-isoquinolyl)carbamoyloxy)ethyl]-N-methylcarboxamide 623.1 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-(2-methyl(4,5,6,7- tetrahydroimidazo[5,4-c]pyridin-5-yl))-4-oxobutyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 639.2 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-[4-(2,2,2- trifluoroethyl)piperazinyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 580.1 (3S)-3-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-4-(N-(3-isoquinolyl)carbamoyloxy)-N-(pyrazin-2- ylmethyl)butanamide 511.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-imidazol-4-ylpropoxy]-N-(3- isoquinolyl)carboxamide 460.1 N-{(1S)-2-amino-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]ethyl}{[(2- chloro-3-fluorophenyl)methyl]amino}-N-methylcarboxamide 562.1 N-[(1S)-1-(4-hydroimidazo[1,5-a]pyrazin-3-ylmethyl)-2-(N-(3- isoquinolyl)carbamoyloxy)ethyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 599.3 N-{(1S)-4-(4-acetylpiperazinyl)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 574.2 N-{(1S)-4-(3-fluoropiperidyl)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 590.1 {N-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3- isoquinolyl)carbamoyloxy)propyl]carbamoyloxy}ethyl acetate 571.2 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-(2- oxopiperazinyl)butyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 558.1 N-[(1S)-4-amino-3,3-difluoro-1-({N-[5-(3-fluorophenyl)isoxazol-3- yl]carbamoyloxy}methyl)butyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 584.1 N-[(1S)-5-diazo-3,3-difluoro-1-({N-[5-(3-fluorophenyl)isoxazol-3- yl]carbamoyloxy}methyl)-5-azapent-5-enyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 584.0 N-[(1S)-5-diazo-3,3-difluoro-1-({N-[3-(3-fluorophenyl)isoxazol-5- yl]carbamoyloxy}methyl)-5-azapent-5-enyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 558.1 N-[(1S)-4-amino-3,3-difluoro-1-({N-[3-(3-fluorophenyl)isoxazol-5- yl]carbamoyloxy}methyl)butyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 566.1 N-[(1S)-1-(imidazo[1,5-a]piperazin-3-ylmethyl)-2-(N-(3- isoquinolyl)carbamoyloxy)ethyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 537.1 N-[(1S)-1-({N-[3-(3-fluorophenyl)isoxazol-5-yl]carbamoyloxy}methyl)- 3-hydroxy-3-methylbutyl]{[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 558.0 [(2S)-3-[(2,2-difluoroethyl)amino]-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)propoxy]-N-[5-(3- fluorophenyl)isoxazol-3-yl]carboxamide 540.1 [(2S)-3-[(2,2-difluoroethyl)amino]-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)propoxy]-N-(5- phenylisoxazol-3-yl)carboxamide 558.1 [(2S)-3-[(2,2-difluoroethyl)amino]-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)propoxy]-N-[3-(3- fluorophenyl)isoxazol-5-yl]carboxamide 540.1 [(2S)-3-[(2,2-difluoroethyl)amino]-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)propoxy]-N-(3- phenylisoxazol-5-yl)carboxamide 743.0 [(2S)-3-(N-(2,2-difluoroethyl){[(2-chloro-3- fluorophenyl)methyl]amino}carbonylamino)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)propoxy]-N-[3-(3- fluorophenyl)isoxazol-5-yl]carbo 725.1 [(2S)-3-(N-(2,2-difluoroethyl){[(2-chloro-3- fluorophenyl)methyl]amino}carbonylamino)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)propoxy]-N-(3- phenylisoxazol-5-yl)carboxamide 745.0 [(2S)-3-(N-(2,2-difluoroethyl){[(2-chloro-3- fluorophenyl)methyl]amino}carbonylamino)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)propoxy]-N-[5-(3- fluorophenyl)isoxazol-3-yl]carbo 725.0 [(2S)-3-(N-(2,2-difluoroethyl){[(2-chloro-3- fluorophenyl)methyl]amino}carbonylamino)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)propoxy]-N-(5- phenylisoxazol-3-yl)carboxamide 499.1 N-[(1R,2R)-2-(N-(3-isoquinolyl)carbamoyloxy)cyclohexyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-ethylcarboxamide 494.1 N-[(1S)-2-amino-1-({N-[5-(3-fluorophenyl)isoxazol-3- yl]carbamoyloxy}methyl)ethyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 431.1 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-[2-(N-(3- isoquinolyl)carbamoyloxy)ethyl]-N-methylcarboxamide 485.1 N-[(1S,2S)-2-(N-(3-isoquinolyl)carbamoyloxy)cyclohexyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 471.1 N-[(2S,1R)-2-(N-(3-isoquinolyl)carbamoyloxy)cyclopentyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 471.1 N-[(1S,2S)-2-(N-(3-isoquinolyl)carbamoyloxy)cyclopentyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 504.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-[(2-hydroxyethyl)amino]propoxy]-N-(3- isoquinolyl)carboxamide 548.1 [(2S)-3-[bis(2-hydroxyethyl)amino]-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)propoxy]-N-(3- isoquinolyl)carboxamide 499.0 [2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-[1-(trifluoromethyl)(3- isoquinolyl)]carboxamide 499.0 [2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)ethoxy]-N-[4-(trifluoromethyl)(3- isoquinolyl)]carboxamide 476.1 [(2S)-3-amino-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-(5-phenylisoxazol-3-yl)carboxamide 602.0 [(2S)-3-amino-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-(4-iodo-5-phenylisoxazol-3- yl)carboxamide 619.9 [(2S)-3-amino-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)propoxy]-N-[5-(3-fluorophenyl)-4-iodoisoxazol-3- yl]carboxamide 647.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[4-(methylethyl)piperazinyl]-5-oxopentyloxy]- N-[5-(3-fluorophenyl)isoxazol-3-yl]carboxamide 629.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[4-(methylethyl)piperazinyl]-5-oxopentyloxy]- N-(5-phenylisoxazol-3-yl)carboxamide 647.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[4-(methylethyl)piperazinyl]-5-oxopentyloxy]- N-[3-(3-fluorophenyl)isoxazol-5-yl]carboxamide 619.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(4-methylpiperazinyl)-5-oxopentyloxy]-N-[3-(3- fluorophenyl)isoxazol-5-yl]carboxamide 459.1 [3-({[(2-chloro-3-fluorophenyl)methyl]amino}-N-methylcarbonylamino)- 2-methylpropoxy]-N-(3-isoquinolyl)carboxamide 457.0 N-{(2S,1R)-2-[(N-(3- isoquinolyl)carbamoyloxy)methyl]cyclopropyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 491.1 [((2S)-1-{N-[(2-chloro-3-fluorophenyl)methyl]carbamoyl}pyrrolidin-2- yl)methoxy]-N-[3-(3-fluorophenyl)isoxazol-5-yl]carboxamide 459.1 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-[2-(N-(3- isoquinolyl)carbamoyloxy)-1-methylpropyl]-N-methylcarboxamide 445.1 {[(2-chloro-3-fluorophenyl)methyl]amino}-N-[2-(N-(3- isoquinolyl)carbamoyloxy)-1-methylpropyl]carboxamide 584.1 N-((1S)-3-{3-[(dimethylamino)methyl](1,2,4-oxadiazol-5-yl)}-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]propyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 599.1 N-{(1S)-4-(4-ethylpiperazinyl)-1-[(N-(3- isoquinolyl)carbamoyloxy)methyl]-4-oxobutyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 613.1 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-oxo-4-(4- propylpiperazinyl)butyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 627.1 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-[4-(2- methylpropyl)piperazinyl]-4-oxobutyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 541.1 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-3-(3-methyl(1,2,4- oxadiazol-5-yl))propyl}{[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarboxamide 653.1 N-{(1S)-1-[(N-(3-isoquinolyl)carbamoyloxy)methyl]-4-[4-(2,2,2- trifluoroethyl)(1,4-diazaperhydroepinyl)]butyl}{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 629.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-[4-(methylethyl)piperazinyl]-5-oxopentyloxy]- N-(3-phenylisoxazol-5-yl)carboxamide 619.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(4-methylpiperazinyl)-5-oxopentyloxy]-N-[5-(3- fluorophenyl)isoxazol-3-yl]carboxamide 601.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(4-methylpiperazinyl)-5-oxopentyloxy]-N-(5- phenylisoxazol-3-yl)carboxamide 444.0 N-((1S)-2-amino-1-{[N-(5-chloro(2- pyridyl))carbamoyloxy]methyl}ethyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 585.2 [5-((3R)-3-methylpiperazinyl)(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-oxopentyloxy]- N-(3-isoquinolyl)carboxamide 585.2 [(2S)-5-((3S)-3-methylpiperazinyl)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-oxopentyloxy]- N-(3-isoquinolyl)carboxamide 585.2 [(2S)-5-((2S)-2-methylpiperazinyl)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-oxopentyloxy]- N-(3-isoquinolyl)carboxamide 585.1 [5-((2R)-2-methylpiperazinyl)(2S)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-oxopentyloxy]- N-(3-isoquinolyl)carboxamide 599.1 [(2S)-5-(3,5-dimethylpiperazinyl)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-oxopentyloxy]- N-(3-isoquinolyl)carboxamide 599.1 [(2S)-5-((3S,5R)-3,5-dimethylpiperazinyl)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-oxopentyloxy]- N-(3-isoquinolyl)carboxamide 611.1 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(4-cyclopropylpiperazinyl)-5-oxopentyloxy]-N- (3-isoquinolyl)carboxamide 625.2 [(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-5-(4-cyclobutylpiperazinyl)-5-oxopentyloxy]-N- (3-isoquinolyl)carboxamide 576 N-[(2S)-2-({[(2-chloro-3-fluorophenyl)methyl]amino}-N- methylcarbonylamino)-3-(N-(3-isoquinolyl)carbamoyloxy)propyl]-3- hydroxy-2-(hydroxymethyl)-2-methylpropanamide 510 N-[(1S)-2-amino-1-({N-[3-(3-chlorophenyl)isoxazol-5- yl]carbamoyloxy}methyl)ethyl]{[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide 599.2 [(2S)-5-(3,3-dimethylpiperazinyl)-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-oxopentyloxy]- N-(3-isoquinolyl)carboxamide 639.1 [(2S)-5-[(2S)-2-(trifluoromethyl)piperazinyl]-2-({[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarbonylamino)-5-oxopentyloxy]- N-(3-isoquinolyl)carboxamide 644.1 N-((1S)-2-{N-[3-(3-chlorophenyl)isoxazol-5-yl]carbamoyloxy}-1- {[(phenylmethoxy)carbonylamino]methyl}ethyl){[(2-chloro-3- fluorophenyl)methyl]amino}-N-methylcarboxamide

While the present invention has been described with reference to the specific embodiments thereof, it should be understood by those skilled in the art that various changes may be made and equivalents may be substituted without departing from the true spirit and scope of the invention. In addition, many modifications may be made to adapt a particular situation, material, composition of matter, process, process step or steps, to the objective, spirit and scope of the present invention. All such modifications are intended to be within the scope of the claims appended hereto. 

What is claimed is:
 1. A compound of Formula I

or a pharmaceutically acceptable salt thereof, wherein W¹ is O; W² is NR¹³; W³ is NR¹⁴; Z¹ is selected from isoquinolinyl, thiadiazolyl, and isoxazolyl; Z² is phenyl; R⁸ is selected from hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, and optionally substituted heterocycloalkyl; R¹³ and R¹⁴ are independently selected from hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, and optionally substituted heterocycloalkyl; for each occurrence, R³, R⁴, and R⁵ are independently selected from hydrogen, hydroxy, carboxy, sulfonyl, sulfinyl, sulfanyl, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted alkoxy, optionally substituted aryloxy, optionally substituted heteroaryloxy, optionally substituted heterocycloalkyloxy, optionally substituted aminocarbonyloxy, optionally substituted acyloxy, optionally substituted alkoxycarbonyloxy, optionally substituted acyl, optionally substituted alkoxycarbonyl, optionally substituted amino, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aminocarbonyl, and optionally substituted aminosulfonyl; R⁷ and R¹⁰ are independently selected from hydrogen, cyano, halo, hydroxy, azido, nitro, carboxy, sulfinyl, sulfanyl, optionally substituted alkoxy, optionally substituted aryloxy, optionally substituted heteroaryloxy, optionally substituted heterocycloalkyloxy, optionally substituted alkoxycarbonyl, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted aryloxy, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted heterocycloalkyl, optionally substituted amino, optionally substituted acyl, optionally substituted alkoxycarbonyl, optionally substituted aminocarbonyl, optionally substituted aminosulfonyl, optionally substituted carbaminodoyl, and optionally substituted alkynyl; m is selected from 0, 1, 2, and 3; n is selected from 0, 1, 2, 3, and 4; —(CR⁵R⁶)_(q)— is —CH₂CH(R⁵)—; and p is selected from 0, 1, 2, and
 3. 2. The compound of claim 1 wherein R¹³ is selected from hydrogen and optionally substituted lower alkyl.
 3. The compound of claim 2 wherein R¹³ is hydrogen.
 4. The compound of claim 1 wherein R¹⁴ is selected from hydrogen and optionally substituted lower alkyl.
 5. The compound of claim 4 wherein R¹⁴ is selected from hydrogen, lower alkyl, and lower alkyl substituted with one or two groups selected from hydroxy, optionally substituted amino, and optionally substituted alkoxy.
 6. The compound of claim 5 wherein R¹⁴ is selected from hydrogen, methyl, ethyl, propyl, and isopropyl, wherein methyl, ethyl, propyl, and isopropyl are optionally substituted with one or two groups selected from hydroxy, optionally substituted amino, and optionally substituted alkoxy.
 7. The compound of claim 6 wherein R¹⁴ is selected from hydrogen, methyl, ethyl, propyl, and isopropyl, wherein methyl, ethyl, propyl, and isopropyl are optionally substituted with one or two hydroxy groups.
 8. The compound of claim 7 wherein R¹⁴ is selected from methyl, ethyl, hydroxymethyl, 2-hydroxyethyl, and isopropyl.
 9. The compound of claim 8 wherein R¹⁴ is selected from methyl and ethyl.
 10. The compound of claim 1 wherein R⁸ is selected from hydrogen and optionally substituted lower alkyl.
 11. The compound of claim 10 wherein R⁸ is selected from hydrogen and methyl.
 12. The compound of claim 11 wherein in R⁸ is hydrogen.
 13. The compound of claim 1 wherein R⁵ is selected from hydrogen, optionally substituted lower alkyl, and optionally substituted alkenyl.
 14. The compound of claim 1 wherein W² is NH and R¹⁴ is methyl.
 15. The compound of claim 1 wherein m is
 0. 16. The compound of claim 1 wherein m is selected from 1 and 2, and each R⁷ is selected from halo and optionally substituted alkyl.
 17. The compound of claim 16 wherein each R⁷ is selected from chloro, fluoro, and methyl.
 18. The compound of claim 17 wherein —(R⁷)_(m), together with Z² to which it is attached, forms a group selected from 2-chlorophenyl, 2-methylphenyl, 2-chloro-4-fluorophenyl, 2-chloro-3-fluorophenyl, 2,3-dichlorophenyl, 2,3-difluorophenyl, 2,4-dichlorophenyl, 2,4-difluorophenyl, and 3-chloro-2-fluorophenyl.
 19. The compound of claim 1 wherein n is
 1. 20. The compound of claim 19 wherein each R³ and R⁴ is independently selected from hydrogen and optionally substituted lower alkyl.
 21. The compound of claim 20 wherein each R³ and R⁴ is hydrogen.
 22. The compound of claim 1 wherein p is selected from 0, 1, and 2, and R¹⁰ is selected from halo, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted heterocycloalkyl, and optionally substituted aryl.
 23. The compound of claim 1 wherein p is 0 and Z¹ is isoquinolin-3-yl.
 24. The compound of claim 1 wherein Z¹ is isoquinolin-3-yl, p is selected from 1 and 2, and each R¹⁰ is independently selected from halo.
 25. The compound of claim 1 wherein Z¹ is isoxazol-5-yl, p is 1, and R¹⁰ is selected from optionally substituted phenyl.
 26. The compound of claim 1 wherein Z¹ is isoxazol-3-yl, p is 1, and R¹⁰ is selected from optionally substituted phenyl.
 27. The compound of claim 1 wherein Z¹ is 1,3,4-thiadiazol-2-yl, p is 1, and R¹⁰ is selected from optionally substituted phenyl.
 28. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and at least one compound of claim
 1. 29. A pharmaceutical composition of claim 28 wherein the composition is formulated in a form selected from a tablet, capsule, powder, liquid, suspension, suppository, and aerosol.
 30. The compound of claim 13 wherein R⁵ is lower alkyl substituted with one, two, or three groups selected from 4-(lower alkyl)piperazin-1-yl, oxopiperazin-1-yl, morpholino, benzyloxy, benzyloxycarbonyl, methoxycarbonyl, hydroxy, amino, dimethylamino, methoxy(methyl)carbamoyl, acetamido, acetyl, azido, phosphato and halo.
 31. The compound of claim 30 wherein R⁵ is lower alkyl substituted with one, two, or three groups selected from hydroxy and phosphato.
 32. The compound of claim 31 wherein R⁵ is lower alkyl substituted with one, two, or three groups selected from hydroxy and —OP(O)(OH)₂.
 33. The compound of claim 32 wherein R⁵ is lower alkyl substituted with —OP(O)(OH)₂ and optionally further substituted with one or two hydroxy groups.
 34. The compound of claim 13 wherein R⁵ is lower alkyl substituted with optionally substituted heteroaryl.
 35. The compound of claim 34 wherein R⁵ is lower alkyl substituted with imidazol-4-yl, imidazol-2-yl, pyridin-2-yl, 1,2,4-oxadiazol-5-yl, isoxazol-5-yl, imidazo[1,5-a]piperazin-3-yl, or 4-hydroimidazo[1,5-a]pyrazin-3-yl, each of which is optionally substituted.
 36. The compound of claim 13 wherein R⁵ is lower alkyl substituted with optionally substitute aminocarbonyl.
 37. A compound of Formula I

or a pharmaceutically acceptable salt thereof, wherein W¹ is O; W² is NR¹³; W³ is NR¹⁴; Z¹ is selected from isoquinolinyl, thiadiazolyl, and isoxazolyl; Z² is phenyl; R³ is hydrogen; R⁴ is hydrogen; —(CR⁵R⁸)_(g)— is —CH₂CH(R⁵)—; R⁵ is lower alkyl substituted with one, two, or three groups selected from hydroxy and phosphato; R⁷ and R¹⁰ are independently selected from hydrogen, cyano, halo, hydroxy, azido, nitro, carboxy, sulfinyl, sulfanyl, optionally substituted alkoxy, optionally substituted aryloxy, optionally substituted heteroaryloxy, optionally substituted heterocycloalkyloxy, optionally substituted alkoxycarbonyl, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted aryloxy, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted heterocycloalkyl, optionally substituted amino, optionally substituted acyl, optionally substituted alkoxycarbonyl, optionally substituted aminocarbonyl, optionally substituted aminosulfonyl, optionally substituted carbaminodoyl, and optionally substituted alkynyl; R⁸ is selected from hydrogen and alkyl; R¹³ and R¹⁴ are independently selected from hydrogen and alkyl; m is selected from 0, 1, 2, and 3; n is 1; and p is selected from 0, 1, 2, and
 3. 38. The compound of claim 37, wherein R⁵ is lower alkyl substituted with one or two groups selected from hydroxy and —OP(O)(OH)₂.
 39. The compound of claim 38, wherein m is selected from 1 and 2, and each R⁷ is selected from halo and optionally substituted alkyl.
 40. The compound of claim 39 wherein —(R⁷)_(m) together with Z² to which it is attached form a group selected from 2-chlorophenyl, 2-methylphenyl, 2-chloro-4-fluorophenyl, 2-chloro-3-fluorophenyl, 2,3-dichlorophenyl, 2,3-difluorophenyl, 2,4-dichlorophenyl, 2,4-difluorophenyl, and 3-chloro-2-fluorophenyl.
 41. The compound of claim 40, wherein p is 0 and Z¹ is isoquinolin-3-yl.
 42. The compound of claim 40, wherein Z¹ is isoquinolin-3-yl, p is selected from 1 and 2, and each R¹⁰ is independently selected from halo.
 43. The compound of claim 40, wherein Z¹ is isoxazol-5-yl, p is 1, and R¹⁰ is selected from optionally substituted phenyl.
 44. The compound of claim 40, wherein Z¹ is isoxazol-3-yl, p is 1, and R¹⁰ is selected from optionally substituted phenyl.
 45. The compound of claim 40, wherein Z¹ is 1,3,4-thiadiazol-2-yl, p is 1, and R¹⁰ is selected from optionally substituted phenyl. 